Healthcare & life sciences jobs

12,910 open roles across pharma, biotech, medical devices, and clinical research.

Product Manager UX Orchestration

Jobgether

**This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Product Manager UX Orchestration based in United Kingdom.** This is a strategic product leadership role focused on making complex advertising technology simple, scalable, and self\-serve for publishers. You will own the no\-code configuration layer across ad formats, video players, consent management, paywalls, and related publisher experiences. Your work will directly influence how quickly customers activate, configure, and adopt the platform without engineering support. You will shape consistent experiences across back\-office tools, client\-facing interfaces, native platforms, and WordPress environments. The role combines product strategy, UX thinking, systems design, and close collaboration with engineering and design teams. You will also champion an AI\-native approach, ensuring capabilities are designed to work for both human users and intelligent agents. In a fast\-moving, data\-driven environment, you will have significant scope to simplify processes and turn configuration into a meaningful growth driver. **Accountabilities** * Define the no\-code configuration strategy, including clear boundaries between self\-serve and internally managed capabilities. * Own the roadmap for ad\-format activation and tagging, enabling publishers to configure formats independently and reducing reliance on developers. * Continuously simplify configuration journeys to remove friction, improve adoption, and reduce support demand. * Own the configuration experience for video player templates, including customization of player behavior and appearance. * Lead the evolution of video catalog management capabilities covering uploads, organization, metadata, and scalability. * Own the CMP and paywall template configuration layer, ensuring consistent experiences across applicable surfaces. * Establish cross\-surface UX consistency across back\-office tools, client\-facing platforms, native experiences, and WordPress. * Promote consistent use of design\-system patterns and maintain clear data contracts and access\-control rules for configuration actions. * Apply an agentic\-first product philosophy, ensuring capabilities available through the UI can also be executed by AI agents. * Audit existing workflows to identify gaps between human and agent capabilities and prioritize the most valuable opportunities for improvement. * Partner with Account, Product, Design, Compliance, and Engineering teams to deliver reliable, scalable, and intuitive configuration tools. * Contribute to a culture of pragmatic problem\-solving, prioritization, transparency, and continuous improvement. **Requirements** * 3\+ years of Product Management experience, ideally within self\-serve platforms, admin or back\-office products, no\-code tools, or configuration\-heavy products. * Strong UX sensibility and a demonstrated ability to transform complex configuration processes into simple, intuitive, guided experiences. * Solid technical literacy, including familiarity with API\-first product design and WordPress plugin environments; coding expertise is not required. * Strong systems\-thinking capabilities, with the ability to create frameworks, guardrails, permission models, and scalable product structures rather than isolated features. * Experience coordinating across multiple product or engineering teams where successful delivery depends on strong cross\-functional alignment. * An agentic mindset, with an understanding of AI tool\-calling patterns and the ability to define clean, well\-scoped interfaces that agents can execute. * Familiarity with AdTech, advertising\-format activation, video players, CMPs, consent management, or related technologies is a strong advantage. * Excellent communication skills, with the ability to align technical, design, product, and client\-facing stakeholders around a shared vision. * Strong analytical and pragmatic problem\-solving skills, with a natural ability to challenge established processes and focus on high\-impact outcomes. * An AI\-native approach to product thinking, including the ability to translate business complexity into structured documentation, logic, workflows, and operational blueprints that intelligent systems can execute. * Comfortable working in a fast\-paced environment and applying principles such as Pareto prioritization to focus effort where it creates the greatest impact. * Curious, collaborative, adaptable, and receptive to feedback, with a strong willingness to continuously learn and improve. **Benefits** * Fully remote working environment with flexibility to work from wherever you are most productive. * Access to urban office locations in Paris, Lille, or London when in\-person collaboration is preferred. * Collaborative, close\-knit international team environment focused on innovation and mutual support. * Regular social events and team activities designed to strengthen connections and celebrate achievements. * Opportunity to contribute to a rapidly growing technology business shaping the European digital advertising landscape. * Career development support through training programs, HR career check\-ins, internal mobility opportunities, and regular performance feedback. * Comprehensive health and pension benefits designed to support employees and their families. * Inclusive workplace committed to equal opportunities **How Jobgether Works** We use an **AI\-powered matching process** to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top\-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? **Data Privacy Notice:** By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre\-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Healthtech & Digital Health

Territory Sales Manager, Joint Replacement – Greater Manchester

Stryker

Lancashire, England, UK

**Territory Sales Manager – Greater Manchester** Joint Replacement \- manual and robotic Are you driven and results oriented? Do you have a passion for building long term relationships with customers and improving patient outcomes? Are you looking to be part of a motivated, high performing team for a market leader in the medical technology industry? If so, we want to hear from you. **Job Description** We’re looking for a talented, highly motivated sales professional who will be responsible for driving Stryker’s Joint Replacement and Robotics business in Greater Manchester. As part of a high calibre, performance driven sales team, you must have a passion for delivering results, improving outcomes and making the lives of patients better. This is not just a job; it is a career where you can grow, be developed and gain organisational influence by taking a path which can move in many different directions. Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in Orthopaedics, Medical and Surgical, Neurotechnology and Spine that help improve patient and hospital outcomes. **Key Responsibilities** * Developing an effective territory sales strategy to drive growth. * Delivering annual sales targets as well as other key performance objectives. * Building strong relationships with a diverse group of stakeholders in the NHS \& private medical sector; these include, consultants, theatre managers, nursing staff as well as procurement and finance professionals. * Grow the utilization of the Mako system by increasing volume with current and potential surgeons. * Provide complete reports and associated metrics to management and regulatory department. * Conducting trials and evaluations of product in theatre and clinical environment to drive sales. * Providing in theatre product support for manual cases. * Working effectively as a part of a team. * Attending and participating in key professional congresses and events * Maintaining and acquiring new product, technology, market knowledge. **Experience \& Competencies** * Positive attitude, a "can do" solution orientated approach to succeed. * Self\-motivated, you take ownership of your work and need no prompting to drive your learning, productivity, change, and outcomes. * Collaborative partners, you build and leverage relationships to bring together ideas, data and insights to drive continuous improvements and ultimately to secure wins within your own team as well as in other teams/functions across the business. Teamwork is an integral part of this role. * Goal Orientated, to thrive in this fast\-paced environment you will stop at nothing to ensure you achieve your goals, keeping the patient/customer and their requirements in focus, we want people who deliver safe and robust solutions. * High Ethics \& Integrity, we want you to win in the right way, that’s a fundamental building block of Stryker’s vision. * Excellent communication and presentation skills * Excellent written and oral skills * 3\+ years successful sales experience in medical devices or healthcare industry preferred * Working knowledge of the NHS, selling in a theatre environment or experience in Medical Devices, would be an advantage, but not essential. * Strengths in accordance with Gallup profile * This role reports into the Regional Sales Manager North West \& Northern Ireland. Ideally the candidate should be located in the Greater Manchester area. **United Kingdom Pay Ranges:** * United Kingdom: £38,600 \- £64,300 GBP Annual At Stryker, we believe transparency helps candidates make confident decisions about their next career step. Compensation is an important part of that process and we want to be clear about how pay is determined. The compensation information posted for this role may be presented as a salary range or a fixed amount depending on the role. In addition to base salary, this role may be eligible for incentive compensation (such as bonus and/or commissions where applicable), along with Stryker’s comprehensive benefits package. If you’d like to learn more about the salary or the benefits associated with this role, your recruiter will be happy to walk you through the details as you progress through the hiring process. Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.

Medical Device

Software Engineer

Medical Engineers Recruitment

Leeds, England, UK

Most software engineers spend their careers building things that never leave a screen. This one won't be like that. A Leeds\-based robotics MedTech company has built a sedation\-free colonoscopy device: magnetic, single\-use, born out of a decade of research at the University of Leeds. It's already running in human clinical trials. The heart of this role is a fully custom embedded Linux distribution, not a standard build, and you'll own it. Alongside that, you'll get hands\-on with the robotic manipulation algorithms steering the scope itself, and help set the coding standards a growing team will build on. **What the role actually involves:** * Maintaining and evolving a custom Linux distro on the edge platform, genuinely core to the role * Contributing to the robotic algorithms that guide the device * Some ownership of the front\-end/UI layer * Setting the coding conventions the rest of the team follows * Working close to the hardware, not just abstracted software * Doing it properly with structured Git workflow, real lifecycle discipline **What you'll need:** * Significant depth in custom embedded Linux (Yocto knowledge a bonus) * Some background in robotic or mechatronic systems * Comfortable with Git and structured software delivery * C/C\+\+ and embedded systems exposure * UI experience is a plus, not a requirement Strong graduates with a relevant placement or gap year are just as welcome here as experienced engineers.

Healthtech & Digital Health

National Account Manager

STADA Thornton & Ross

Location not specified

STADA UK Thornton \& Ross is on an exciting growth journey with more than 700 employees being fully committed to our purpose of Caring for People’s Health as a Trusted Partner. Together we are shaping the future of Thornton \& Ross by living our values of Integrity, Entrepreneurship, Agility and One STADA. **STADA UK \|Thornton \& Ross \| National Account Manager** **Remote / Work from home contract \|U.K.\| Full\-time \| Permanent** Step into a high\-impact National Account Manager role where you’ll shape the success of some of the UK’s best\-known consumer healthcare brands. Working in the dynamic Pharmacy Channel across STADA UK’s Thornton \& Ross and Natures Aid portfolios, you’ll own strategic relationships with major national accounts – driving profitable sales, spearheading new product launches, and maximising brand visibility in\-store. You’ll lead larger channel customers, build and execute strategic account plans, negotiate commercial agreements, and deliver against ambitious business objectives. Reporting to the Channel Controller and working closely with a Senior NAM, you’ll have clear support for your development and progression, while also playing a key role in coaching and supporting key account managers across the team. If you’re a commercially sharp account manager ready to take ownership of sales fundamentals – from profit and distribution to promotional activity and customer engagement – this role puts you at the heart of STADA’s growth in UK pharmacy. **How You Will Make An Impact** * Own customer and market data to unlock opportunities, spot risks, and build Joint Business Plans that grow sales, share, and brand visibility. * Drive profitable growth by securing smart promotions, optimising prices and investment, and winning incremental opportunities for STADA UK in the Pharmacy Channel. * Shape customer strategy by influencing retail buyers on must\-stock lines, ranges, merchandising and NPD, backed by compelling performance stories and insight. * Be the trusted face of STADA: build strong relationships across buyers, supply chain, regulatory and internal teams, championing the customer and STADA’s mission and values. * Deliver best\-in\-class account management through accurate forecasting, budget control, promotion evaluation, and rigorous stewardship that meets all legal and compliance standards. * Consistently exceed sales, market share and profit targets while achieving personal objectives and contributing to STADA UK’s reputation in the UK OTC healthcare industry. **What We Are Looking For** * Proven track record in national account management, sales or commercial roles with major UK customers, ideally in OTC and the Pharmacy channel. * Sharp commercial mind: strong financial acumen, analytical skills and high proficiency in Excel and PowerPoint. * Advanced negotiation and influencing ability, backed by excellent communication and presentation skills. * Strategic, creative and critical thinker, able to plan effectively, manage projects and juggle multiple priorities independently. * Collaborative, diligent and resilient team player with a strong customer focus. * Mobile and field\-ready, holding a full UK driving licence **How We Care For You** At Natures Aid our purpose “Caring for people’s health as a trusted partner” motivates us every day. And what would be a better place than starting with our own employees. Which is why we give much in return: 💸 Competitive salary, car allowance and annual bonus scheme. 🗝 Salary Sacrifice Pension Scheme offering 6% employer contribution rates. ⌚ Remote working – you can expect 2\-3 UK based business trips per month to customer sites and our offices in Preston / Huddersfield / Reading. 🌴 25 days of annual leave plus bank holidays with the potential to buy up to 5 additional days. 🏥 Health benefits provided through our Vitality Private Medical Insurance 💉 Free winter flu jab. 🧠 Wellbeing support through our Employee Assistance Programme and KYAN Wellbeing – offering free coaching and counselling services for you and your family. ⚡ Salary sacrifice Tech\-Scheme. 🚲 Cycle to Work Scheme. 👪 Enhanced Family Leave. 🎉 Plus, many more employee benefits \& celebration events. *STADA Group values and promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology, or sexual orientation. We use the strength of our uniqueness to develop creative ideas, expand our experience and increase innovative strength. Our focus is on equal opportunities, respectful cooperation, and the promotion of an inclusive working environment. We are looking forward to your application and welcome applications without a pharmaceutical background.* – MN1

Medical Device

Territory Sales Manager, Joint Replacement – Greater Manchester

Stryker

Crewe, England, UK

Medical Device

DM/STDM Programmer

IQVIA

Reading, England, UK

Possible Location: UK, Spain, Belgium, South Africa, Romania, Hungary, Ireland, France, Italy, Czech Republic, Bulgaria. This unique role within IQVIA lends itself to a technically minded person with strong communication skills and SDTM knowledge. Having experience in Study Design, CRF annotation, CDISC standards, Vendor management with SAS programming skills will be key for this position. The role can be based remotely from anywhere in Europe or in South Africa. This role is part of a sponsor dedicated project where you will be working with the client directly to manage Database CRF and SDTM Deliveries. The primary functions of this role will be to oversight all activities related to SDTM end to end. Including the management of CRF design from the protocol, ensuring Vendors specifications are compliant with SDTM needs and defining SDTM specification on some studies and/or SDTM review and oversight, ensuring quality and completeness of SDTM format data. **Main Responsibilities Include** * Collaborate with Sponsor colleagues and CRO Partners to review CRF design and compliance into standard and SDTM. * In collaboration with Study Data Leads ensure the planning for data receipt and its oversight throughout the duration of assigned clinical trials * Program reports and contribute to the standardization of process and reports used for data review and analysis for external partners/vendors and internal teams * Complete formal and ad\-hoc analyses and oversight of SDTM data. * Review of critical document/deliverable (SDTM Annotation, SDTM datasets) to ensure Data Standards are used consistently and support creation of DE dataset * Map SDTM data and manage annotated CRF * Attend meetings as applicable with Mission, Submission, Project, Program, JCST, DEM, Biometrics, Clinical \& Regulatory Solutions Team (CRST), Early Phase * Perform relevant quality checks and create standard edit checks for new CRF modules and share in the appropriate space * Support audits and inspections as required and other responsibilities and projects that the Company may assign. **Experience** * At least 5 years relevant in either SDTM and/or CRF design * Experience with Biometrics processes to include: * Review of SDTM annotated CRFs * Writing and reviewing technical specifications * Review of log files for errors and warnings * Resolving/trouble shooting errors * Experience with data mapping and SDTM Controlled Terminology * Experience with SAS programming and SDTM deliveries * Prior experience in a clinical or pharmaceutical related field is required. * Prior experience in a Data Management related field is required * Experience with relational databases, preferably Clinical Data Management and EDC Systems * Advanced familiarity with reporting tools. * Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices. * Excellent command, both verbal and written, of English IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Healthtech & Digital Health

Director, Translational Data Enablement

AstraZeneca

Cambridge, England, UK

**Location:** This role can be based in **Cambridge, UK** , or **Munich, Germany** . We're building a connected, end\-to\-end Enterprise AI engine \- uniting data foundations, AI technology, process reinvention, and business\-facing AI to accelerate results across the whole value chain. Success depends on being exceptional connectors: you'll actively leverage existing capabilities, celebrate and promote reuse, export breakthrough ideas across geographies and functions, and obsess over scaling impact rather than building in isolation. If you thrive in high\-collaboration environments where your role is to turn complex, cross\-functional problems into reusable, enterprise\-wide capabilities \- and where the measure of success is adoption and scale, not just innovation \- you'll have the platform (and sponsorship) to make it real. Own the transformation of translational and biomarker data into AI\-ready, standardized data products that accelerate drug discovery and development. The role sits at the critical intersection of science teams (who generate and use the data), technology teams (who build platforms and automation), and peer data leadership across clinical trial submission and preclinical/discovery domains. Primary mandate: deliver high\-quality, reusable data products while building capabilities to enable a AI ready and FAIR end to end data flow. Lead a 12–15 person distributed team and coordinate cross\-functionally with peer Directors to ensure enterprise\-wide data coherence and strategy alignment. **Key Responsibilities** Science Enablement \& Delivery * Own delivery of analysis\-ready datasets to science teams, enabling precision medicine, biomarker discovery, and hypothesis validation * Work with science stakeholders to understand analytics needs and shape data standards accordingly * Create data catalogs, metadata standards, and usage guidelines; establish feedback mechanisms for continuous improvement Standards \& Data Product Strategy * Define FAIR\-compliant standards for translational/biomarker data (omics, imaging, proteomics, etc.). Establish quality frameworks and SLAs aligned to regulatory, AI/ML, and precision medicine use cases * Build semantic schemas and harmonization layers enabling integration of data from diverse sources (labs, vendors, partners) into reusable, consumable data products Platform \& Technology * Define technical requirements for translational data workflows (ingestion, validation, harmonization, delivery APIs) * Lead automation initiatives to reduce manual curation (e.g., schema\-driven harmonization, intelligent quality assurance). Measure efficiency gains * Ensure integration with enterprise systems (clinical data lakes, AI/ML platforms) * Pilot new technologies (agentic AI, ML\-driven quality assurance) at scale Team Leadership \& Cross\-Domain Coordination * Recruit, mentor, and scale a 12–15 person distributed team of data stewards and engineers responsible for data curation, validation, and delivery * Partner with other team leads on shared deliveries, leveraging synergies and cont. increasing efficiency Strategic Leadership * Define multi\-year roadmap for expanding translational/biomarker data standardization across therapeutic areas and partners * Drive shift from reactive data cleanup to proactive "Shift Left" data generation * Present at industry forums; own P\&L for translational data operations **Required Experience \& Qualifications** * PhD or master degree in bioinformatics, biomedical data science, molecular medicine, or related field * Published research or thought leadership on biomarker standardization, data harmonization, and data product build and delivery with 5\+ years experience * Experience with leading a cross functional, global team including budget oversight, hiring, onboarding * Experience with FAIR data principles, semantic interoperability, or data standards in research contexts (GA4GH, MIAME, etc.) * Track record scaling data governance or data stewardship programs across multiple labs, studies, or organizations * Familiarity with agentic AI, machine learning, or LLM\-driven automation in data/science workflows * Familiarity with biomarker platform companies (e.g., Guardant Health, Foundation Medicine, Tempus) or research consortia (e.g., NCI's SEQC, GTEx) *Ready to lead the transformation of healthcare through AI? Join us in building the platform that will power the next generation of life\-changing medicines and make a meaningful impact on patients' lives worldwide.* When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life\-changing medicines. In\-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, we are driven by a shared purpose to make a difference in patients' lives through innovation and collaboration. Our dynamic environment encourages continuous learning and growth as we explore new technologies and challenge conventional approaches. By partnering across functions and leveraging our data capabilities, we empower our teams to achieve remarkable outcomes. Join us as we shape the future of healthcare and contribute to AstraZeneca's mission of delivering life\-changing medicines. **\#EAI** **Date Posted** 26\-ago\-2026 **Closing Date** 15\-sept\-2026 Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.

Pharma & Biotech

256774 - Medical Education Training Co-ordinator

NHS Scotland

Wishaw, Scotland, UK

**About The Organisation** Here at NHS Lanarkshire, we put the patient at the heart of everything we do. Each colleague within the organisation plays a key role in how we deliver our healthcare services. We proudly serve a population of 655,000 across rural and urban communities in both North and South Lanarkshire. NHS Lanarkshire is comprised of Acute Services (which currently provide hospital based services over 3 main sites), Corporate \& Property \& Support Services, North and South Lanarkshire Health and Social Care Partnerships which provide integrated primary healthcare and social care services to local communities and surrounding areas. **The Role** Managing the co\-ordination, planning, compilation and implementation of Medical Education Training Programmes for all Consultants, Staff Grades, Associates Specialists, Junior Doctors, GPs and Medical Students throughout NHS Lanarkshire and all subsequent business and project administration ensuring maximum marketing and advertising. **In This Key Role, You Will** Producing, undertaking all relevant research/duties and implementing a yearly training calendar for all Clinicians ensuring that all costs fall within allocated budget, spreading events throughout the year and taking into consideration external factors that may hinder attendance(exam dates, etc) to ensure delegates have maximum ability to attend for training and managing the co\-ordination of the Major Annual Symposium Sourcing, reviewing and negotiating with course providers obtaining relevant details/data regarding courses commissioning of providers, effective management of accommodation \- viewing, deciding on and arranging course venues and organising hospitality \- ensuring all is within budget. Liaising and negotiating with sponsors for course (both prior to and on day) to manage fee support and stand positions Producing and acting on annual Training Needs Analysis and department activity report – research, content \& formatting. Managing the overseeing of report production and liaising with printing companies as required, before co\-ordinating its distribution to Senior clinicians **What You'll Bring** The post holder must possess working knowledge of a full range of Senior Administration, Business and Training procedures acquired through training to HND Level with relevant experience within a training environment and/or Business Administration environment. This is vital to carry out duties. Advanced keyboard skills/qualifications and an in\-depth working knowledge and lengthy experience of complex IT packages are required including Microsoft Publisher, Excel, Word, Outlook, Project, Access, Powerpoint, electronic Diaries/Calendars and in the independent analysis of statistical data and producing publications in various formats for end users. The post holder must have the ability to work autonomously; managing and prioritising own workload within the agreed overall target schedule. The ability to be self\-motivated, flexible, pro\-active and to possess multi\-tasking, interpersonal, time management and forward planning skills is vital. Excellent Communication, negotiation, influencing and motivational skills/training and the ability to deal with and diffuse difficult situations/interactions are required. **What We Offer** As a valued employee of NHS Lanarkshire, you can enjoy an extensive range of benefits including: * Annual Leave \- 35 days including public holidays * Generous NHS pension scheme * Annual incremental salary progression * Paid sick leave increasing with length of service * NHS discounts and more. *NHS Lanarkshire is dedicated to building a diverse workforce where everyone can thrive, develop, and succeed based on their skills, knowledge, and talent \- regardless of race, disability, gender, sexual orientation, or care experience\* or any other dimension that can be used to differentiate people from one another.* * Care experienced applicants include those who have lived with foster parents, kinship carers, or in residential/secure children’s settings. **For informal discussion, please contact Caroline Burke, Directorate Support Manager on Caroline.Burke@lanarkshire.scot.nhs.uk** **If you have any questions about the recruitment process or require support with your application, contact Gemma Irwin, Recruitment Administrator on gemma.irwin@lanarkshire.scot.nhs.uk** **Interested?** Full details about the role are provided in the attached Job Description and Person Specification. Please review our Application Guidance which explain key information including closing dates, amendments, right‑to‑work requirements, sponsorship eligibility and important points to be aware of before submitting your application You can also learn more about working with NHS Lanarkshire by viewing our Information Pack Unless otherwise stated, the deadline for applications is 23:59 hours on the closing date. **Please note, CVs will not be accepted.** **This advert may close early if we receive a high number of applications, so we encourage you to apply early.**

Healthtech & Digital Health

Principal Scientist, Pharmaceutical Development

IQVIA

Cambridge, England, UK

**Are you an ambitious scientist with expertise in developability, drug delivery or pharmaceutical development, with an interest in applying digital and AI\-enabled approaches to help molecules progress from discovery towards medicines?** **Do you want to help turn promising molecules into medicines by working across developability science, formulation strategy and integrated drug discovery?** Following our integration into IQVIA Laboratories, Pharmaceutical Development is entering an exciting new phase. We are building a modern, developability\-focused scientific function that combines physicochemical sciences, biopharmaceutics, solid\-state science, drug delivery expertise and data\-enabled approaches, to help clients make better decisions and accelerate candidate progression. We are seeking a Principal Scientist in Pharmaceutical Development, to help drive our scientific ambition, shape the future of our discipline, and play a key role in delivering innovative solutions for clients across the global pharmaceutical and biotechnology sectors. The successful candidate will help embed developability thinking earlier in drug discovery programmes, using experimental, computational and AI\-enabled approaches to identify risks, generate insight and support clear recommendations for clients. **Why Join Us?** At IQVIA, Pharmaceutical Development is evolving. We're moving beyond traditional formulation support and building a science\-led capability focused on understanding and mitigating developability risk, enabling confident progression of drug candidates from discovery into development. You'll join a growing team in Cambridge, working alongside experts across Discovery, DMPK, CMC and broader IQVIA scientific functions. **This Is a Role For Someone Who** * Wants to influence scientific direction, not simply execute studies. * Is comfortable challenging the status quo, bringing forward and championing new ideas. * Is interested in using AI\-enabled and data\-driven approaches responsibly to enhance developability assessment, scientific interpretation and client impact. * Enjoys solving complex drug delivery and developability challenges. * Is excited by working directly with clients. * Loves mentoring and developing scientists. * Wants to help shape a growing scientific capability during a transformational period. **What You'll Be Doing** You will combine scientific leadership, client engagement and project delivery responsibilities. * Design, oversee and interpret developability studies to support candidate progression. * Integrate physicochemical, solid\-state, biopharmaceutic and formulation data to inform key development decisions. * Apply digital, computational and AI\-enabled approaches to support developability risk assessment, literature insight, data interpretation and experimental prioritisation. * Translate AI\-supported and experimental insights into clear, scientifically robust recommendations for drug discovery teams and client programmes. * Recommend formulation and development strategies for challenging molecules. * Provide scientific leadership within multidisciplinary drug discovery programmes. * Lead pharmaceutical development projects from proposal through delivery. * Act as the primary scientific contact for client programmes. * Lead and support business development through scientific proposals, technical discussions and client interactions. * Mentor and develop junior scientists. * Contribute to the continued growth and evolution of the Pharmaceutical Development group. **What We're Looking For** We're less interested in finding someone who has done the exact same role before and more interested in finding someone with the curiosity, energy and scientific drive to help us build something exciting. **The Strongest Candidates Are Likely To Bring** * Significant industrial experience in pharmaceutical development or drug discovery, with a broad cross\-disciplinary understanding of the drug discovery process. * Experience designing and interpreting developability, preformulation or formulation studies. * Strong understanding of physicochemical, biopharmaceutic and drug delivery principles. * The ability to integrate experimental, computational, predictive and AI\-enabled approaches to support developability decision\-making. * A track record of leading scientific projects and influencing project direction. * Excellent communication and client\-facing skills. * A passion for scientific problem solving, mentoring and continuous improvement. **What Makes This Opportunity Different?** You’ll be joining at a unique moment. Backed by the global reach and capabilities of IQVIA, we are redefining the role of Pharmaceutical Development within drug discovery. This is your chance to help build a growing scientific function, influence how we work, and contribute to a long\-term vision focused on developability science, innovation and client impact. If you're looking for an opportunity where your scientific expertise, ambition and ideas can genuinely influence the future direction of a team, we'd love to hear from you. **Core Skills And Experience** * A postgraduate degree (BSc/MSc or PhD) in Pharmaceutical Sciences, Chemistry or a related discipline. * Extensive experience of working in an industrial R\&D setting, supporting developability assessment, drug delivery and candidate progression for novel small molecule APIs, within multidisciplinary drug discovery programmes. * Strong knowledge of the drug discovery and development process. * Experience of mentoring junior colleagues. * Ability to communicate complex scientific data to stakeholders with varying degrees of expertise. * A proactive can\-do approach, attention to detail and the ability to adapt to changing demands and requirements. * Scientific project management. **Additional Experience In The Following Approaches Would Be Valuable** * Model\-informed and data\-driven formulation design. * Computational, predictive and AI\-enabled developability approaches. * Ability to interpret PK data and use it to inform formulation and candidate selection strategies. * Application of mechanistic developability approaches (e.g. DCS, PBPK or related modelling frameworks). * Physicochemical characterisation and developability assessment. * Solubility, dissolution and absorption risk evaluation. * Integration of experimental, computational and predictive data to support decision making. * Enabling formulation technologies (e.g. spray drying, particle engineering, lipid\-based systems). * Oral drug delivery and absorption enhancement strategies. * Working knowledge of solid form characterisation techniques. * Experience of supporting non\-oral dosage routes (nasal, inhaled, dermal or parenteral). * Experience addressing developability challenges of Beyond Rule of 5 compounds. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Public Health, Policy & Government

Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)

IQVIA

Reading, England, UK

**Job Overview** Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. Position may be responsible for the implementation of smaller programs in their entirety. Communicate with sponsors and project teams to implement and monitor impact of the recruitment/retention tactical plan; make additional operational and tactical recommendations as needed based on study performance. Collaborate with internal teams and external providers to deliver all appropriate tactics associated with the recruitment/retention strategy. Represent IQVIA Patient Recruitment at site/sponsor\-facing meetings (i.e. KOM, IM, F2F/LL, etc.) to present strategy/rationale, train CRAs and site staff, and conduct recruitment support workshops as required. Ownership for study KPI and financial performance. **Essential Functions** * Work together with strategy team to translate recruitment and retention strategy into operational and tactical plans to positively impact recruitment and retention rates for assigned projects * Serve as internal consultant to project teams to implement operational recruitment plans on new and/or existing projects needing recruitment and retention services * Manage the scope of work, objectives, quality of deliverables, and other activities of assigned projects (based on scope, may co\-manage or independently manage these projects) * Serve as primary operational project contact for patient recruitment and retention programs with sponsor to ensure appropriate communication channels are maintained and reporting schedules adhered to as required * Management of assigned project budget(s) to meet financial and company goals (realization targets) * Coordinate operational and tactical related project activities for study team and sponsor to ensure that overall project milestones are met * Develop and implement risk management plans for minimizing impact on project objectives and deliverables * Other duties as assigned by Management * Maintain knowledge of current recruitment trends, vendors, and technologies to increase productivity and recommend additional support as needed * Leverage internal intelligence to support and refine strategy on assigned projects * Provide technical expertise as able in support of project specific and interdepartmental training efforts * Support continued process improvement to ensure quality in the department * Performing executional task to manage vendors and patient advocacy groups ( e.g. vendor budgets, totality, PO requests, change orders, contracting compliance submission invoice reconciliations, etc) * Liasing with vendor accoutn manager to ensure impact tracking on PSE activities and corresponding digital assets * Ensuring timely PSE related updates to data systems (e.g., DEICT dasboard, vTMF); supporting PSE manager in pulling relevant reports. * Coordinating schedules among internal and external stakeholders to suppport meetings planning for PSE activities. * Undertaking logistical components for congress/conference planning for R\&D activities. * Participating in cross \- DU PSE forums/community of practice to share learning and best practices. **Qualifications** * Bachelor's Degree Health care or other scientific discipline or educational equivalent Req * 6 yrs. of relevant industry experience. Equivalent combination of education, training and experience. * In depth knowledge of the drug development processes across all functional areas * Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines * Excellent organizational and problem solving skills * Effective time management skills and ability to manage competing priorities * Strong interpersonal skills effective presentation skills * Ability to establish and maintain effective working relationships with coworkers, managers and clients * Computer skills including proficiency in aspects of data analysis and presentation software, Microsoft Word, and Excel * Good written and verbal communication skills including good command of English * Ability to influence effectively within SPN/PRP team and project teams including TSL, PL, CL, CRA and the customer The candidate may be based in any EMEA country, as long as their time zone is no more than six hours ahead of US Eastern Time. Candidates located beyond this range are also welcome to apply, provided they are willing to work later hours approximately 80% of the time to support collaboration with US\-based teams. * Please note This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Research

Scientific Team Lead/Director

Assignment Consulting

London Area, United Kingdom

The agency is a forward thinking established company with a strong track record of innovation. There are opportunities for people with agency experience in medical affairs and publications backgrounds. If you have medical communications agency writing/scientific experience across a range of outputs please apply. Remote or hybrid position.

Public Health, Policy & Government

Forensic Investigations Manager

RSM UK

Edinburgh, Scotland, UK

As one of the world's largest networks of audit, tax and consulting firms, RSM delivers big ideas and premium service to help middle\-market businesses thrive. We are a fast\-growing firm with big ambitions \- we have a clear goal to become the premium adviser to the middle market, globally. This vision touches everything we do, motivating and inspiring us to become better every day. If you are looking for a firm where you can build a future and make an impact, then RSM is the place for you. Our Forensic team is growing, and we're looking for an experienced investigations professional to join us as a Manager/Managing Consultant. In this role, you'll work on a wide range of complex and often high\-profile investigations, helping clients navigate fraud, misconduct, financial irregularities and regulatory enquiries. You'll play a key role in delivering projects, managing workstreams and building trusted relationships with clients, legal advisers and other stakeholders. Whether your background is in forensic accounting, corporate investigations, regulatory enforcement or law enforcement, this is an opportunity to develop your expertise within a collaborative and fast\-growing team. **You will make an impact by** You'll take ownership of investigative workstreams while supporting the successful delivery of end\-to\-end engagements. Working closely with senior leaders, you'll help clients understand complex issues, identify risks and deliver robust outcomes. **Responsibilities will include** * Delivering investigations involving fraud, misconduct, financial irregularities and regulatory matters. * Planning, managing and executing investigative workstreams. * Analysing financial and non\-financial information to identify key findings. * Producing clear, structured and high\-quality reports and client deliverables. * Supporting client meetings and stakeholder engagement. * Coaching and developing junior team members. * Contributing to business development activities and the continued growth of the Investigations practice. **What we are looking for** We're keen to hear from motivated professionals who enjoy solving complex problems and delivering exceptional client service. **You'll likely have** * Experience in forensic investigations including into, fraud, misconduct or, financial crime, or related investigative work. * Experience managing elements of investigations and delivering high\-quality client work. * A background in forensic accounting, corporate investigations, internal investigations, regulatory bodies or law enforcement. * A professional qualification (such as ACA, or equivalent) and/or significant investigative experience. Additional qualifications (such as CFE or similar) would be advantageous. * Strong analytical, communication and report\-writing skills. * The ability to manage competing priorities and work effectively in a fast\-paced environment. * A collaborative approach and a passion for developing others. * An interest in getting involved in business development activities. **What we can offer you** We recognise that our people are our most important assets. That’s why we offer a flexible reward and benefits package that will help you have fulfilling experience, both in and out of work. * Hybrid and Flexible working . * 27 Days Holiday (with the option of purchasing additional days) * Lifestyle, Health, and Wellbeing including financial wellbeing benefits such as financial tools, electric car scheme and access to a virtual GP. * Access to a suite of 300\+ courses on demand developed by our inhouse Talent Development team. **Diversity and Inclusion at RSM** At RSM, we want to create a strong sense of belonging so that people of all identities, backgrounds, and cultures feel they can bring their true self to work. Our clients come from all walks of life. We aim to achieve that same diversity of background, experience and perspective in our own teams, so that we can genuinely understand our client's needs. Diverse teams bring a broader range of ideas and insights to work. That's why we're working together to ensure our firm's principles and processes support a firm culture that embraces difference and strengthens inclusion. At RSM we work hard to create an environment where our people can make a difference \- to themselves, their career, their teams, and to the success of our firm and clients. We support all our people to work flexibly, to manage their family and other responsibilities alongside their work commitments; we believe this is key to achieving an inspiring and fulfilling working environment.

Pharma & Biotech

Senior Set-Up Coordinator

IQVIA

Livingston, Scotland, UK

**IQIVIA Laboratories** **Home\-based, office\-based, hybrid options available** IQVIA Laboratories is a global leader in drug discovery and development laboratory services, offering a comprehensive suite of central laboratory and specialty biomarker services. Our expertise spans genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine assays, vaccine assays, ADME, and bioanalytical services. IQVIA Laboratories also specializes in antibody and biomarker discovery, as well as decentralized clinical trial laboratory solutions. Committed to scientific rigor and operational excellence, we support every phase of the drug development and discovery process across diverse regions and regulatory frameworks, ensuring the highest standards of data integrity and accelerating the delivery of transformative therapies to patients. **Join us on our exciting journey!** **Job Overview** Manage the end‑to‑end design and implementation of **protocol amendments and sponsor‑driven changes** , ensuring alignment with system capabilities and regulatory requirements. Identify and apply **AI‑enabled tools, automation, and data analytics** to improve study set‑up efficiency, data quality, and amendment delivery. Lead the design, configuration, and validation of laboratory databases and study set‑up activities using **advanced Clinical Trial Management Systems (CTMS)** and related digital platforms. Communicate effectively with Sponsors and CROs, providing expert input on **technology‑enabled study design and delivery** . Maintain ownership of amendment delivery, sponsor deliverables, and database quality while proactively identifying opportunities to enhance ways of working through **AI, digital transformation, and innovative thinking** . Develop, plans, and delivers laboratory project setup and execution activities across the full study lifecycle, ensuring alignment with sponsor requirements, regulatory standards, and organisational quality expectations. **Requirements** * Bachelor's Degree Life sciences or related field * 1\+ years relevant experience (Clinical, Medical or Healthcare industry preferred) or equivalent combination of education, training and experience. * Demonstrated interest or experience in AI, automation, data analytics, or digital transformation within clinical or laboratory environments. * Strong working knowledge of Clinical Trial Management Systems (CTMS) and laboratory data systems, with the ability to adapt quickly to new technologies. * Comfortable working in fast‑paced, evolving environments where new tools and approaches are continuously introduced. * Curious, proactive, and motivated to explore emerging technologies and innovative solutions. **Join IQVIA to see where your skills can take you** * Global exposure * Variety of therapeutic areas * Collaborative and supportive team environment * Access to cutting\-edge and innovative, in\-house technology * Excellent career development and progression opportunities IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Research

Software Trainer

TAGTRONICS LIMITED

Darwen, England, UK

**Software Trainer** Darwen, Lancashire **About Us** TagCare is a software development company that offers solutions for the homecare sector. Since 2000, we have been developing software and apps to make caring easier, acting as a tailored ‘guiding hand’ for companies that foster a culture of care and driving forward standards across the care industry. Last year marked our 25th anniversary. We are continuously innovating, striving to elevate standards and digital possibilities, enabling those on the frontlines to do their best work. We’re passionate about innovation and the people who use our tools every day, which is why we’re now looking for a Software Trainer to join our friendly team on a full\-time, permanent basis, office\-based (Monday to Friday, 9am–5pm). **The Benefits** \- Salary of up to £35,000 DOE \- Pension \- 25 days’ holiday, plus bank holidays If you are a communications, software trainer, account management, or customer success professional with SaaS expertise, this is the perfect opportunity to join our forward\-thinking organisation. You’ll work in a small, dedicated team where no two days are the same, developing your skills in training, communication, and customer success in a vibrant and rewarding environment. So, if you’re ready to advance your career, we’d love to hear from you! **The Role** As a Software Trainer, you will play a key role in supporting our customers, with your main focus being on training customers on how to use our homecare software, helping them get the most out of the system. You’ll take the lead on onboarding all new clients, guiding them through implementation and delivering tailored training to suit their needs. You’ll also be vital in supporting long\-term success, ensuring customers feel confident and well\-equipped to use our products. Building strong, trusted relationships with your accounts, you’ll be the go\-to person for advice, product guidance, and support. Additionally, you will: \- Support clients through every stage of the onboarding journey \- Deliver training for existing customers and help develop useful training content \- Review customer journeys and identify areas for improvement \- Help clients overcome any challenges using a consultative, solution\-focused approach \- Co\-ordinate with other team members and third\-party providers to keep things on track **About You** To be considered as a Software Trainer, you will need: \- Experience in software training, communications, account management, or customer success \- Experience in SaaS \- Strong skills in verbal and written communications, strategic planning, and project management \- Organisational skills \- To be a team player Other organisations may call this role Software Support Advisor, Account Manager, Software Account Manager, Customer Relationship Manager, Client Relationship Manager, CRM, Stakeholder Relationship Manager, Client Success Manager, or Customer Service Manager. Webrecruit and TagCare are equal opportunities employers, value diversity and are strongly committed to providing equal employment opportunities for all employees and all applicants for employment. Equal opportunities are the only acceptable way to conduct business and we believe that the more inclusive our environments are, the better our work will be. So, if you’re ready to help others succeed through great training and expert support, we’d love to hear from you. Click apply now to join our team as a Software Trainer! This vacancy is being advertised by Webrecruit. The services advertised by Webrecruit are those of an Employment Agency.

Incubators & Accelerators

Recovery Coordinator

Change Grow Live

Broome, England, UK

**Change Grow Live** are a charity dedicated to the belief that we can make a difference to our Service Users lives, offering support and respect in a safe environment, treating each user as an individual and working with them to find the right treatment and care options. Our core values are **‘Be open, be compassionate and be bold’** and our team members apply these daily to achieve our mission of helping people change the direction of their lives, grow as individuals, and live life to its full potential. We have an exciting opportunity for a **Recovery Coordinator** who has the skills and experience to assess and engage with our service users, ensuring that they access the right intervention at the right time, in a way that best meets their needs. No two days are the same and we treat every person who comes into our service as an individual, so being flexible, curious and a good listener are key. **Where** Dudley **Hours** 37\.5 hrs per week **Contract Type** Permanent Full\-time hours at Change Grow Live are 37\.5 hours per week. For part\-time roles, the salary and payments will be pro rata based on contracted hours. About the role * Supporting service users from point of entry into the service and through their treatment/recovery journey * Providing screening, assessment, and recovery planning and onward referral * Reducing drug and alcohol related harm to service users and the wider community * Promoting carer, service user and community involvement * Providing advocacy for access to partnership services * Working with service users to support social (re)integration, enabling them to lead meaningful and purposeful lives promoting recovery, resilience, peer support and self\-determination * Research, design and prepare subject matter and materials for groups / pods. * Deliver structured content within group settings to service users at various stages of recovery * Engage with debriefing and evaluations with co\-facilitators after groups/pods have taken place, reviewing progress and identifying concerns with service users * Tailor specific workshops around the needs of the service users. **About you** * Have a strong understanding of substance misuse issues and experience of working within a similar field * Experience of working with groups/pods and managing group dynamics, such as conflict or challenging behaviour. * Be an excellent communicator, both verbal and written with good IT skills * Proactive and able to work on own initiative with excellent time management and prioritising skills * Have a good working knowledge of mental health interventions, services, and good practice * Be a supportive team player with strong interpersonal skills with the ability to work in partnership with a wide range of professionals, agencies, and internal/external stakeholders * Ability to manage change successfully in a way that prioritises the needs of service users * Understand the importance of information governance processes and commit to follow and apply all necessary safeguards * Seek out learning opportunities to improve and broaden your professional knowledge and skills and to contribute and oversee the learning and development of others **What we will give to you** * 25 days of annual leave, plus bank holidays. Additionally, you'll receive one extra day of annual leave for each year of service during your first five years, therefore you will enjoy 30 days of leave after five years with us * Paid ‘Wellness’ hour each week along with a ‘Wellness’ hub and Employee Assist Programme * Contributory pension scheme * Several benefits incl. discounts for shopping, cinema, holidays, etc. * A friendly and supportive team * Training, career development \& progression opportunities * Generous Refer\-a\-Friend scheme **A Note About Using AI In Your Application** AI can be a really helpful tool when putting together your application, and we're happy for you to use it. However, what we're most interested in is **you** . We want to understand your experiences, achievements and strengths, so please make sure your application reflects your own story and clearly shows how you meet the essential criteria and the impact you've made in previous roles. There's no need to write in a particular style. The strongest applications are authentic, specific and clearly demonstrate your skills, experience and potential. **We look forward to learning more about you.** **Please ensure that when completing your application form and supporting statement, you reflect on the details outlined in the job description. This will help us understand how your skills and experiences align with the requirements of the role.** **Direct applications only we will not be engaging agencies for this vacancy.** **Please note This role is not eligible for visa sponsorship. Applicants must already have the right to work in the UK at the time of application. For applicants with time\-limited visas, unfortunately, we are unable to support new visa applications or extensions. More information about eligible roles and occupations can be found here** Skilled Worker visa Overview \- GOV.UK We reserve the right to close the vacancy early if we receive a high number of applications, so we encourage you to apply as soon as possible. If this sounds like you and you would like to begin your journey with **Change Grow Live,** then we would love to talk to you. CGL points 23 to 28 (£28,557\.79 \- £32,802\.41\) N/A \- Outside London Weighting Area 2/9/2026 Lisa Bradley \| lisa.bradley@cgl.org.uk \| 01384426120 This post is subject to a Disclosure and Barring Service (DBS) check at an enhanced level.

Incubators & Accelerators

Territory Sales Manager, Joint Replacement – Greater Manchester

Stryker

Nantwich, England, UK

Medical Device

Principal, Regulatory Science and Strategy - Real World Solutions

IQVIA

London, England, UK

IQVIA is focused on using data and science to help healthcare clients find better solutions for their patients. Individuals joining us are assured of a rewarding career in Life Sciences Consulting, with opportunities to address diverse and challenging client problems, contribute to cross\-geography engagements, interact with senior client leaders, and gain exposure to a multicultural and collaborative work environment. **About Our Team – Regulatory Science And Strategy (RSS)** The Regulatory Science and Strategy (RSS) group sits within IQVIA's Real World Solutions business and supports life sciences clients in using real world evidence (RWE) more widely and effectively for regulatory purposes. RSS sells and delivers as a unified team, partnering with clients on regulatory strategy, study design, and submission planning across drugs, biologics, and devices. Our work spans externally controlled trials, post\-marketing requirements (PMRs/PMCs), post\-authorization safety studies (PASS), drug utilization studies (DUS), and emerging regulatory technology. We are strategic thinkers, deep subject matter experts, and creative at our core. We are collaborative, intellectually curious, and entrepreneurial. **About The Role** As a Principal (Director\-level) within RSS, you will own delivery leadership, drive business development, and serve as a subject matter expert across two connected areas: selling and delivering standalone regulatory strategy engagements and cross\-functional RWE studies for regulatory decision\-making. Your work will focus primarily on several areas: First, a Principal is expected to lead high\-quality standalone regulatory strategy engagements, build trusted relationships with new and existing clients, and strengthen IQVIA's regulatory science and strategy capabilities. Second, the Principal acts as a subject matter expert on the use of RWE across the regulatory lifecycle, partnering cross\-functionally with IQVIA Real World Solutions teams to shape, sell, and deliver RWE studies from pre\-submission strategy through approval and post\-market commitments. An in\-depth understanding of EMA expectations is essential, with the ability to translate those expectations into study designs and submission strategies that clients can act on. Specifically, as a member of the RSS team, the Principal participates in regulatory strategy proposal development, advises on regulatory pathways, and supports cross\-functional proposal strategy and delivery for externally controlled trials, PASS, DUS, RegTech advisory work, and broader RWE\-for\-regulatory engagements. In addition we expect you to make a key Team and operational contributions to RSS, including mentorship and capability building amongst your junior colleagues **Responsibilities** * Lead sell and delivery of standalone RSS regulatory strategy engagements, owning workstreams end\-to\-end and supporting team members on complex programs. * Support cross\-functional IQVIA Real World Solutions teams in selling and delivering RWE generation programs for regulatory audiences, including externally controlled trials, premarket uses of RWE, PASS, and PMR/PMC fulfilment. * Contribute to RSS regulatory intelligence activities, monitoring the external regulatory environment and surfacing emerging information relevant to IQVIA's offerings and clients. * Act as a day\-to\-day owner of the regulatory science element of client engagements, with responsibility for client satisfaction and delivery quality. * Advise on strategy and delivery plans for RSS services, with a focus on EMA RWE activities and lifecycle management, supported by working knowledge of FDA, MHRA, Health Canada, and PMDA. * Maintain working familiarity with the activities and outputs of EMA and their impact on global harmonization of RW efforts. * Identify follow\-on work and new revenue opportunities with existing clients, and support business development efforts with new client organizations. * Collaborate across IQVIA when client requirements span regulatory affairs, clinical development, and real world insights. * Provide direction, advice, and intellectual leadership to delivery teams and clients. * Contribute high\-level input to client reports and presentations, and deliver findings to clients directly. * Mentor and coach junior consultants, sharing subject matter expertise to build RSS capability. * Participate in annual performance review processes and in recruitment of new staff. **Skills And Experience** The successful candidate will have a track record of success across most of the following competencies: * Industry and regulatory expertise: Maintains a constant focus on regulators, industry, and client trends in life sciences. Applies this knowledge to active client engagements and to business development. * Real world data expertise: Ability to advise on the design of real world studies to meet regulatory requirements, including externally controlled trials, PASS, PMR fulfillment, etc. * Regulated medical product experience: Ability to speak with senior client stakeholders about EMA requirements, guidance, and expectations, with working knowledge of FDA, MHRA, Health Canada, and PMDA. * Client relationship management and delivery: Day\-to\-day owner of client engagements, focused on client satisfaction and outstanding deliverables, with the ability to manage multiple workstreams in parallel. * Business development: Active contributor to proposal development and pre\-sales meetings for standalone regulatory strategy opportunities and cross\-functional RWE study opportunities with new and existing client organizations. * Solution selling: Ability to identify client pain points and shape custom solutions for life sciences clients. * Communication and executive presence: Expresses ideas clearly and concisely, and tailors messaging to the audience. * Cooperative teamwork: Builds supportive relationships within RSS and across IQVIA, based on trust and respect. * Management of others: Sets clear direction and develops junior team members by delegating appropriately and creating stretch opportunities. * Coping with decision\-making, customer focus, flexibility, influencing, initiative, innovation, planning and organizing, strategic vision, and technological orientation. **Qualifications And Other Requirements** * A strong academic track record in a life science\-related discipline or professional equivalent. A relevant graduate degree (PharmD, PhD, MD, MPH, or MS) is preferred. * At least 7 years of professional experience, with a meaningful portion focused on regulatory science, regulatory strategy, or product review. Prior experience at EMA or another health authority is highly valued. * Previous experience in life sciences consulting or professional services is preferred. * Evidence of consistent career progression. * A track record of project leadership and people development. * Willingness and ability to travel to client locations. * Fluency in English (spoken and written). * Right to live and work in the recruiting country. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Public Health, Policy & Government

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

IQVIA

Reading, England, UK

**IQVIA™** is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. **The Patient Centered Solutions team** **(PCS)** The PCS team leads the industry in the science of measuring the patient experience. We pair strategic consulting expertise with technical scientific knowledge to design and execute scientifically rigorous research that incorporates the patient voice into the development and commercialization of new medicines. This research includes qualitative (e.g., patient interviews, focus groups), quantitative (e.g., clinical outcome assessments (COAs)/patient\-reported outcomes (PROs), preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and physician experiences and expectations of disease and treatment. **Why join?** * Become part of a recognized global leader in patient\-focused research * Keep growing with an organization that encourages and invests in continuous professional and personal development * Apply your business and leadership skills in an entrepreneurial and multi\-disciplinary team * Continue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry * Make a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient\-centric **Role Overview** Within PCS, the **Qualitative Research Specialty** **(QRS)** delivers scientifically rigorous qualitative research to inform clinical development, regulatory strategy, and healthcare decision‑making. We are seeking an **Associate Principal / Principal** to join the QRS team, based in the **UK or Europe** , with flexibility for **remote or hybrid working** . This role blends scientific leadership, consulting delivery, and people development. The exact level (Associate Principal or Principal) will depend on experience and demonstrated leadership scope. The role is positioned between project‑level scientific leadership and broader practice‑level contribution, with increasing responsibility for client leadership, methodological excellence, business development support, and capability building across the qualitative community. The role has a particular emphasis on generating and applying patient experience data to inform COA development, evaluation, and use within clinical and regulatory contexts. **Key Responsibilities** **Scientific \& Consulting Leadership** * Act as a subject matter expert (SME) in qualitative research, providing expert guidance on study design, methodological approaches, and interpretation of patient experience data, translating findings into evidence that informs COA strategy, endpoint development, and broader clinical and commercial decision\-making across a portfolio of projects spanning in\-trial settings, observational studies, and standalone research programmes. * Lead the design, execution, and delivery of high‑quality qualitative research, including examining burden of disease, evaluating content validity of PROs and other COAs, and the development or modification of COA measures, ensuring scientific rigour, methodological appropriateness, and alignment with regulatory, publication, and client expectations. * Identify, evaluate, and apply innovative qualitative methods, including AI\-enabled approaches, to enhance study design, data collection, and analysis while maintaining scientific rigour. * Lead the review and testing of emerging qualitative research and analysis methods and contribute to the evidence base for their use at PCS. * Provide senior scientific input into qualitative analysis plans, interpretation of patient experience data, and development of reports and client‑facing deliverables. **Project \& Client Management** * Act as a trusted scientific and strategic advisor to clients, contributing to discussions on research design, patient‑centred endpoints, and evidence needs. * Take ownership for overall project quality, delivery, and client satisfaction, ensuring projects remain on track and aligned with scope, timelines, and objectives. * Lead or oversee multiple qualitative consulting projects, ensuring delivery on time, within scope, and to budget. * Serve as a primary or senior point of contact for clients, building strong, long‑term relationships through meetings, workshops, and ongoing collaboration. * Anticipate project risks and proactively resolve issues, escalating as needed while maintaining client confidence. * Support proposal development, including methodological input, budgeting, timelines, and bid integrity. **Practice Development \& Business Growth** * Identify opportunities for follow‑on work, methodological innovation (including the scaling of innovative and AI\-enabled qualitative approaches), and expansion of qualitative service offerings within PCS. * Contribute to thought leadership, including development of best practices, internal guidance, and externally facing scientific content (e.g. abstracts, presentations, publications). * Support business development activities by providing subject‑matter expertise and mentoring others in client and proposal engagement. **Quality, Standards \& Capability Building** * Contribute to the development, refinement, and implementation of qualitative research standards, templates, SOPs, and training materials. * Oversee and contribute to the qualification and ongoing development of qualitative researchers, including assessment of interview moderators. * Support consistency and quality across qualitative projects, working collaboratively with global qualitative leaders (Global Qualitative Research Speciality Leads, Delivery \& Capabilities; Innovation \& Professional Development). * Provide scientific review and guidance to ensure best practice in qualitative data collection, analysis, and reporting. **People Development \& Collaboration** * Mentor and coach junior and mid‑level staff, providing scientific guidance, project oversight, and developmental feedback. * Line manage and formally coach a small number of staff, supporting their scientific development, performance, and career progression, depending on level and business need. * Actively contribute to the global PCS qualitative community, supporting recruitment, onboarding, and knowledge‑sharing initiatives. * Foster a collaborative, inclusive, and high‑performing team culture across geographies. **About You** **Essential Qualifications \& Experience** * PhD in a relevant discipline (e.g. psychology, anthropology, sociology, public health, health sciences) or a Master’s degree with substantial consulting or additional experience. * 5\-8 years professional experience in consulting within the pharmaceutical industry. * Demonstrated expertise in designing, conducting, and analyzing qualitative research in healthcare settings. * Familiar with designing and leading qualitative research consistent with Patient\-Focused Drug Development guidance published by the US FDA. * Experience working in roles generating or communicating robust clinical data suitable for submission to regulatory bodies, payers or for publication; including exposure to the development and validation of COAs. * Experience using qualitative data analysis software (e.g., ATLAS.ti, MAXQDA, NVivo) to support efficient and rigorous coding, analysis and management of qualitative data. * Experience working in consulting or a CRO environment, managing multiple complex projects and senior client stakeholders. * Strong understanding of qualitative methods, analytical approaches, and reporting standards suitable for regulatory, payer, or publication contexts. * Demonstrable analytical, interpretative, and problem\-solving skills, with the ability to learn quickly, adapt, and apply new knowledge. * Strong capability in juggling priorities so that deadlines are met while retaining consistently high\-quality outcomes. * Excellent written and verbal communication skills, including client presentations, workshops, and scientific writing. * Ability to manage and collaborate with individuals at all levels within the organization and build relationships while working remotely. **Desirable Experience (depending On Level)** * Experience contributing to regulatory‑focused research (e.g. clinical trials, endpoint development, patient experience studies). * Track record of publications, abstracts, or conference presentations. * Experience with cross\-cultural or multilingual research design. * Experience contributing to proposal development and business growth. * Formal people management or coaching experience. **Core Competencies** * Scientific curiosity and commitment to methodological excellence. * Strong project and stakeholder management skills. * Ability to translate complex qualitative insights into clear, actionable narratives for clients. * Collaborative mindset with the confidence to provide senior‑level input and challenge constructively. * Excellent organizational skills and ability to balance competing priorities. * Strong client focus, including the ability to lead senior discussions to uncover underlying needs, shape strategic research approaches, and support the growth of client accounts. * Execution excellence, with accountability for high\-quality, on\-time delivery, proactive risk mitigation and oversight of project delivery. * People leadership, demonstrated through mentoring, coaching, and supporting the development of qualitative researchers **Practical Details** * Location: UK or Europe * Working model: Remote or hybrid (office/home‑based) * Travel: Occasional travel expected * Language: Fluen

Pharma & Biotech

Associate Clinical Project Manager - Sponsor Dedicated

IQVIA

Reading, England, UK

The SSO Clinical Project Manager (CPM) is accountable for the day\-to\-day planning,executing, and reporting, (from first site initiation visit to and including study site close\-out), of assigned studies in compliance with Sponsor processes and regulatory requirements. The CPM is the single point of contact and study team lead, in the country/cluster/hub, for the assigned studies. The CPM is responsible for assuring aligned communication with Trial Leads and other CTT members, locally with Clinical Research Associates (CRAs), CRA Managers and other key associates on the execution and progress of their studies. The CPM collaborates with the SSO Country Manager, SSO Country Head, SSO Feasibility Manager, SSO Study Start\-up Manager and SSO Site Partnership Manager in the planning, execution, and delivery of their assigned studies. Accountable for execution and reporting of assigned studies in E2E product line Clinical Operations Program Head/Study Lead/CPM – CRA. Can be assigned partially to participate in the review process of Site Monitoring Plans across the Portfolio. **Responsabilities** * Supports SSO Study Start\-up Manager with the development of country/cluster/hub study execution plans and timeline commitments. * Participates with the recruitment sub\-team and supports the development of innovative solutions for site and patient participation to ensure the delivery of assigned studies on time * Proactively identifies risks and opportunities for the assigned studies in the country/cluster/hub and develops respective mitigation plans * Supports study feasibility as requested by the SSO Feasibility Manager by providing input to the study protocol and operational aspects of the study * Maintains a strong knowledge of the study protocol to answer standard operational questions from CRAs, sites and Country/Cluster/Hub personnel * Drives the conduct of the study (tracks status, maintains relevant reporting systems, oversees forecasts, progress, and mitigation plans) to ensure all study operational aspects are on track * Ensures recruitment targets are met and reviews enrollment at the site level including responsibility for obtaining approval from the STUDY LEADER on enrolling above site targets. * Responsible to set up contingency plan to ensure recruitment targets are achieved in accordance with trial execution plan * Oversees local study team activities to achieve study timelines and quality execution, (proposing and implementing corrective actions where appropriate), according to Sponsor standards and relevant regulations * Leads/chairs country/cluster/hub study team meetings, participates in global clinical trial team meetings, as required, and is the single point of contact for the conduct of assigned studies * Maintains oversight of country/cluster/hub level data management activities, including timely understanding of screen failure reasons and discontinuation rates, review of patient profiles, and proactively identifies data entry issues (on quality and timing) to mitigate queries, proactively identifies query resolution issues * Coordinates the study handover process with CRAs and their managers to ensure proper documentation and communication, when necessary * Tracks all study close–out activities and ensures they are performed in a timely manner, in collaboration with CRAs and key study stakeholders * Conducts or coordinates training, as needed, for CRAs to support site readiness to recruit and study execution ensuring adherence to clinical data standards, prevailing legislation, GCP, Ethical Committee and SOP requirements * Conducts or coordinates local investigator meetings, as needed, and ensures relevant training documentation is archived in the Trial Master File * Evaluates potential challenges/risks in the protocol and operational aspects of the study; assesses impacts, develops risk management plans, and communicates/escalates to global teams and SSO Hub Head Portfolio, as appropriate * Accountable for monitoring quality and issue resolution through timely review and approval of study monitoring visit reports to ensure quality trial oversight and appropriate issue escalation * Promotes a compliance culture advocating the adherence to highest standards and ethical integrity, ensuring human subject protection and reliability of trial results at all times. * Acts as the escalation point for issues in monitoring visit reports (MVRs) for the assigned studies. * Responsible for evaluating trends identified in MVRs and communicating/escalating these to global teams, as appropriate. Communicates with CRAs and their managers to ensure issue resolution in a timely manner * Provides feedback about the quality of monitoring activities to CRA Managers, MSOM, SSO Country Managers, FSP/BiS line managers, as appropriate, and to local QA (when required per Sponsor SOPs) * Supports inspection readiness and submission preparation for monitoring\-related activities; assists and coordinates with country Portfolio Execution and Quality Assurance for internal audits organization and HA inspections, as required, and ensures implementation of corrective actions within specified timelines. * Monitors the status of site budget and contract negotiations as well as the collection and review of essential documents throughout study conduct. * Tracks study budget with appropriate study budget in responsible Country. Ensures timely TCF preparation and submission. * Processes invoiceable items for site level clinical study activities to allow timely payments * Serves as core member of the Global Clinical Trial team as a Country and Hub representative responsible for all local level feedback to the global trial execution teams. * Interfaces with SSU teams to ensure on\-time initiation of all sites within geography. * Interfaces with Country study execution teams, including CRAs and CRA Managers, to ensure on\-time recruitment, data delivery, and study close out. **Requirements** achelor's Degree Life sciences or related field Req * 5 years of prior relevant experience including \> 1 years project management experience or equivalent combination of education, training and experience. Req * Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience. Req * Knowledge of clinical trials \- Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge; therapeutic knowledge desired. Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.; * Communication \- Strong written and verbal communication skills including good command of English language. Strong presentation skills. * Problem solving \- Strong problem solving skills. * Leadership \- Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently. * Leadership \- Ability to make decisions, bringing clarity to disparate information to inform actions and drive results. * Organisation \- Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances. * Prioritisation \- Ability to handle conflicting priorities. * Quality \- Attention to detail and accuracy in work. Results\-oriented approach to work towards delivery and output. * Quality \- Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving. * IT skills \- Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint. * Collaboration \- Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills. * Cross\-collaboration \- Ability to work across geographies displaying high awareness and understanding of cultural differences. * Finances \- Good understanding of project financials including experience managing, contractual obligations and implications. * IQVIA Core Competencies \- Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership). * Please note This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Research

Advocacy and Recruitment Specialist

Snow Companies

Newcastle Upon Tyne, England, UK

**Agency** Snow **Job Function** Communications and PR **Job Subfunction** Digital Marketing **Job Description** The Advocacy and Recruitment Specialist position operates at the core of the Snow Companies business model. This position is ultimately responsible for the identification and screening of new Patient Ambassadors™ and establishing and maintaining relationships with clinical trial sites and physician offices. The role requires comfort level in strategic planning and establishing oneself as a subject\-matter expert, providing project guidance to the company as a whole. The key transferrable skills for these positions are compassion, communication, organization, and resourcefulness. Snow’s business is centered around the patient journey, and the Advocacy and Recruitment Specialist, like all positions at Snow, must be open, compassionate, and sensitive to the unique life experiences of these patients and caregivers. The Advocacy and Recruitment Specialist must be able to incorporate the unique patient/caregiver experience into the strategies and solutions we provide to our clients. **Required Skills** To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. **Relationship Building And Patient Screening** * Recruiting new patients for candidacy in our Patient Ambassador™ Programs is essential to the existence of the company. * Advocacy and Recruitment Specialists must cultivate relationships with the staff of physicians’ offices, clinics, support groups, and other patient\-focused organizations through a variety of methods and techniques as deemed appropriate and effective. * They must have the ability to be flexible and continually design new recruitment techniques to find eligible Patient Ambassadors™. * They must manage their time effectively to meet the competing needs of all brand teams, coordinate schedules with the rest of the team to insure coverage for our incoming educational hotlines, and be able to manage tight deadlines. * Advocacy and Recruitment Specialists must exercise independent judgment and discretion in determining the best recruitment channels to use, eligibility of potential candidates, and the necessary information and background data to be gathered, all while properly handling sensitive, private health care information. * Recruiting specialists own the flow of their day and must be able to formulate, affect, interpret, and implement management policies and operating practices. * The recruiting team serves as subject\-matter experts on recruiting techniques and strategy, and it provides insight and direction to the company as a whole on best practices and strategic planning. * Team members are required to have a good understanding of patient privacy laws (HIPAA) and adverse event (AE) reporting as well as disease knowledge and sensitivity. * Professionalism is of utmost importance at all times. * Compassion, empathy, time management, and organization are extremely important to successfully fulfill this role. * Collaboration with Account Team members to keep them informed of recruitment status is essential. * Team members collaborate to hire and train new team members. * A strong teamwork mentality is needed for this position. **Language Skills/Communication** Candidates must have the ability to read and comprehend general documents relating to the pharmaceutical/bio\-technology industry that include, but are not limited to, medical education, medical periodicals, clinical trial data, package inserts, medical procedures, and industry regulations. Candidates will have demonstrated their ability to effectively and professionally communicate with managers, clients, customers, Ambassadors, and the general public. Working with patients requires candidates to exercise discretion and empathy as patients are living with chronic conditions. Fluency in a foreign language is a plus. **Organization** Members of the Recruitment and Advocacy Team may be asked to simultaneously manage and drive the recruitment for multiple programs, develop relationships with clinical trial sites and physicians’ offices, screen potential Ambassadors, and aid in developing recruitment plans. Therefore, it is important that these employees have demonstrable organizational skills and can give clear examples of their ability to multitask in a high\-pressure environment. Additionally, recruiting for live programs requires the ability to keep information and materials organized as well as the ability to lead a team to meet recruiting goals. The importance of privacy means that recordkeeping and file management are crucial. **Patient Privacy** The core of our business is working with patients. It is most likely that the selected candidate will come in contact with Personal Consumer Information (PCI) of patients living with chronic illness. It will be required that you take training courses that include, but are not limited to: * Snow Policy Training * Health Insurance Portability and Accountability Act (HIPAA) * Adverse Event (AE) Reporting Training * U.S. Food and Drug Administration (FDA) Training **Resourcefulness** Recruitment and Advocacy management inherently requires a person to “think on their feet.” A demonstrated ability to anticipate hurdles and overcome them quickly and effectively is paramount. **Collaboration/Teamwork** The size and nature of our company will require that candidates work in collaboration with people in other departments. Candidates must demonstrate their willingness/ability to step into other roles as needed to drive the success of the company. Candidates will need to demonstrate their ability to be a contributing member of a team that has goals that are broader than an individual job description or function. **Education And Experience** Bachelor's degree (B.A.) from a four\-year college or university, or three to five years of related experience, or equivalent combination of education and experience preferred. MPH, RN, or LPN preferred. *Omnicom’s policy requires employees to work in the office for a minimum of three days a week, unless additional in\-office days are directed by their agency or manager. Our objective is to increase this requirement over time, and many of our agencies as well as Omnicom’s corporate group already require five days of in\-office attendance.* Omnicom is committed to hiring and developing exceptional talent. We agree that talent is uniquely distributed, and we’re focused on developing inclusive teams that can bring the best solutions to everything we do. We strongly believe that celebrating what makes us different makes us better together. Join us—we look forward to getting to know you. We will process your personal data in accordance with our Recruitment Privacy Notice. Link to Recruitment Privacy Notice: https://www.omc.com/privacy\-notice **For US Job Seekers** *It is the policy of Omnicom and any of its affiliates to provide equal employment opportunities to all employees and applicants for employment without regard to race, religion, color, ethnic origin, gender, gender identity, age, marital status, veteran status, sexual orientation, disability, or any other basis prohibited by applicable federal, state, or local law. EOE/AA/M/D/V/F.*

Pharma & Biotech

Research Fellow - School of Engineering - 107860 - Grade 7

University of Birmingham

Birmingham, England, UK

**Job Description** **Position Details** School of Engineering Location: University of Birmingham, Edgbaston, Birmingham UK Full time starting salary is normally in the range £36,636 to £46,049 with potential progression once in post to £48,822 Grade: 7 Full Time, Fixed Term contract up to June 2028 Closing date: 17th September 2026 **Background** This role is part of the philanthropically funded programme to develop a rapid, highly sensitive test for early\-stage bladder cancer. The multidisciplinary project involves developing methods to increase the specificity of an optical biosensor to detect bladder\-cancer\-associated DNA targets. The programme brings together expertise in nucleic\-acid chemistry, molecular diagnostics, photonic sensing, engineering and bladder\-cancer research. The research fellow will lead the design, statistical optimisation and validation of assays for clinically relevant bladder cancer targets. Their central objective will be to develop an algorithmic workflow to detect new target sequences, achieving rapid detection at femtomolar concentrations whilst maintaining robust separation between true\-positive and negative reactions. The post\-holder will work closely with research fellow will work across the School of Medicine, School of Chemistry, and School of engineering to integrate the statistically optimised assay into a photonics diagnostic workflow. **Role Summary** * Lead the development and optimisation of biomolecular assays for bladder\-cancer\-associated DNA variants. * Apply a range of algorithmic approaches to quantitative modelling to improve assay sensitivity, specificity, speed and positive\-negative separation. * Design and validate assays for single\-nucleotide variants and low\-abundance variant alleles in a wild\-type DNA background. * Characterise analytical performance, including limit of detection, selectivity, specificity, reproducibility, time\-to\-detection and false\-positive behaviour. * Translate optimised reactions from synthetic targets to urine\-derived DNA. * Collaborate with the photonic sensing and surface functionalisation teams to integrate the assay with the photonics biosensor. * Write to publications, grant applications, intellectual\-property protection, research supervision and project reporting. **Main Duties** The responsibilities will focus on rapidly developing robust nucleic\-acid amplification assays and integrating them with the transducers used by the photonics diagnostic platform. The work will include: * Designing oligonucleotides and biomolecular reactions for bladder\-cancer\-associated targets, which are being identified by the medical school. * Develop, optimise and validate assays that provide rapid detection, very low limits of detection and clear separation between target\-positive and negative reactions. * Use structured statistical methods to study reaction variables dependence on oligonucleotide sequence and concentration, enzyme concentrations, buffer composition, temperature, incubation time and other relevant factors. * Develop and apply statistical and ML approaches to accelerate optimisation of new biomolecular assays. * Design and evaluate sequence\-selective assays for single\-nucleotide variants, including detection of low variant allele fractions in mixtures containing an excess of wild\-type DNA. * Compare and analyse amplification data from fluorescence\-based with label\-free photonics sensor readouts. * Quantify assay performance using appropriate metrics, including time\-to\-threshold, limit of detection, sensitivity, specificity, selectivity, false\-positive rate, reproducibility, dynamic range and receiver\-operating\-characteristic analysis. * Investigate reaction failure modes, non\-specific amplification and matrix effects, and implement appropriate controls, contamination\-prevention procedures and troubleshooting strategies. * Establish workflows that progress from synthetic oligonucleotides to extracted DNA, urine\-derived samples and clinically relevant materials, in accordance with ethics, biosafety and data\-governance requirements. * Work with engineering researchers to integrate biomolecular reactions with microfluidic handling, temperature control and the optical biosensor. * Develop reproducible experimental protocols, data\-analysis scripts and user\-facing workflows that support efficient transfer of optimised assays to new target sequences. * Maintain accurate laboratory records, version\-controlled analysis files, risk assessments, reagent inventories and project documentation, and ensure that research data are managed in accordance with University requirements. * Analyse and interpret research findings, identify the next most informative experiments and adapt the research plan to address technical problems and project deadlines. * Prepare research outputs, including manuscripts, conference presentations, technical reports and contributions to funding applications. * Contribute to protection and translation of intellectual property and to appropriate enterprise or knowledge\-exchange activities arising from the research. * Provide day\-to\-day guidance to students or research staff contributing to the project and coordinate work across the collaborating disciplines. * Contribute to School research activities and administration, foster a fair and equitable workplace, and identify and respond appropriately to equality and diversity matters in line with University policies. **Person Specification** **Essential Criteria** * A PhD awarded or near completion in biochemistry, molecular biology, chemical biology, biotechnology, nucleic\-acid diagnostics or a closely related discipline, or equivalent PhD\-level research experience. * Substantial hands\-on experience in the design, development and optimisation of nucleic\-acid amplification assays, including direct practical experience with isothermal techniques. * Demonstrable experience using statistical melthods to optimise multi\-parameter biochemical or nucleic\-acid amplification reactions. * Experience applying Machine Learning to optimise and guide iterative laboratory experiments. * Experience of oligonucleotide design and of adapting an amplification method to new target sequences. * Experience developing sequence\-selective assays for single\-nucleotide variants or closely related sequence\-discrimination problems. * Experience analysing amplification kinetics and evaluating assay performance, including limit of detection, sensitivity, specificity, selectivity, positive\-negative separation and false\-positive behaviour. * Strong practical molecular\-biology skills, including PCR/qPCR, nucleic\-acid handling and purification, restriction\-enzyme methods, gel electrophoresis and plate\-reader or spectrophotometric assays. * High\-level quantitative and analytical capability, with experience using statistical and ML packages with a Python programming environment. * Ability to troubleshoot complex biochemical assays, identify causes of non\-specific amplification and design appropriate controls. * Ability to plan and deliver an experimental programme independently, coordinate work with collaborators and use laboratory resources effectively. * Ability to communicate complex scientific information clearly in written and oral form and to prepare publication\-quality data and research outputs. * Ability to work effectively within a multidisciplinary team spanning molecular science, engineering, data analysis and clinical research. * Knowledge of the protected characteristics and duties under the Equality Act 2010, including fostering good relations and advancing the University's Public Sector Equality Duty. **Desirable criteria** * Evidence of achieving ultra\-low nucleic\-acid detection limits, ideally in the attomolar concentration range, while retaining a clear distinction between positive and negative reactions. * Evidence of substantially improving the analytical sensitivity or robustness of a biomolecular assay through systematic experimental optimisation. * Experience detecting low\-frequency single\-nucleotide variants in mixtures containing a large excess of wild\-type DNA. * Experience working with urine, clinical samples, wastewater or other complex biological matrices. * Knowledge of integrating nucleic\-acid amplification with a non\-fluorescent photonics detection method. * Experience of research translation, intellectual property, a diagnostics start\-up, industrial collaboration or grant writing. * Experience supervising undergraduate or postgraduate laboratory projects and contributing to multidisciplinary project management. * Evidence of scientific publication, conference presentation or successful research communication. * Evidence of effective working and collaborating across different schools. I.e. interdisciplinary working Informal enquiries to Robert Simpson, email: r.e.simpson.1@bham.ac.uk View our staff values and behaviours here ***Use of AI in applications:** We want to understand your genuine interest in the role and for the written elements of your application to accurately reflect your own communication style. Applications that rely too heavily on AI tools can appear generic and lack the detail we need to assess your skills and experience. Such applications will unlikely be progressed to interview.* **We believe there is no such thing as a 'typical' member of University of Birmingham staff and that diversity in its many forms is a strength that underpins the exchange of ideas, innovation and debate at the heart of University life. We are committed to proactively addressing the barriers experienced by some groups in our community and are proud to hold Athena SWAN, Race Equality Charter and Disability Confident accreditations. We have an Equality Diversity and Inclusion Centre that focuses on continu

Academia

AI Native Startup Manager

NVIDIA

Location not specified

NVIDIA has been transforming computer graphics, PC gaming, and accelerated computing for more than 25 years. It’s a unique legacy of innovation that’s fueled by great technology—and amazing people. Today, we’re tapping into the unlimited potential of AI to define the next era of computing. An era in which our GPU acts as the brains of computers, robots, and self\-driving cars that can understand the world. Doing what’s never been done before takes vision, innovation, and the world’s best talent. As an NVIDIAN, you’ll be immersed in a diverse, supportive environment where everyone is inspired to do their best work. Come join the team and see how you can make a lasting impact on the world. We are looking for an AI Native Startup Partner Managers to join NVIDIA for Startups — NVIDIA’s business got startups building on NVIDIA technologies across AI, accelerated data science, high\-performance computing, and advanced visual computing. **What You’ll Be Doing** * Identify, engage, technically assess, and recruit the most relevant and promising startups across Europe building on NVIDIA\-accelerated platforms, with a focus on Media \& Entertainment, LegalTech, AI Developer Tools, Data Science, and Generative AI * Evaluate startup technical maturity, architecture decisions, and platform alignment, including usage of CUDA libraries, NVIDIA SDKs, AI frameworks, GPU\-accelerated data pipelines, and training/inference stacks * Share ecosystem, technology, and developer\-level insights with internal partners, translating startup feedback into actionable input for NVIDIA platform, SDK, and product teams * Act as the voice of NVIDIA Inception members by developing a deep understanding of their technical roadmaps, research foundations, system architectures, and platform dependencies * Provide AI Native priority members with technically relevant content, enablement, and tooling to accelerate adoption of CUDA\-based libraries, NVIDIA SDKs, AI frameworks, and developer platforms * Design and lead one\-to\-few technical workshops, briefings, and deep dives in collaboration with Solutions Architects and Developer Relations, focused on accelerating time\-to\-production and platform optimization on NVIDIA technologies * Work closely with the venture capital ecosystem to surface technically differentiated startups, share investment\-grade technical insights, and support portfolio companies with compute, infrastructure, and platform strategy * Support sell\-to and sell\-with motions in alignment with NVIDIA sales teams, channel partners, and startups’ enterprise customers, particularly where GPU acceleration, CUDA performance, and platform differentiation are central to the value proposition **What We Need To See** * 8\+ years of professional experience in related fields such as startup accelerators or incubators, executive or senior roles at technology startups, platform ecosystem development at large technology companies, or venture capital with a strong technology focus * Bachelor’s degree or equivalent experience in Computer Science, Engineering, Mathematics, Physics, or a related technical field; advanced degrees are a plus * Strong affinity for AI, machine learning, data science, and accelerated computing, with working familiarity across CUDA, GPU architectures, NVIDIA SDKs, and modern AI tooling * Ability to engage credibly with technical founders, engineering leaders, and researchers, and to translate complex platform concepts into clear, actionable guidance * Excellent interpersonal skills; comfortable working across a broad ecosystem of startup founders, researchers, investors, and NVIDIA internal teams * Strong written and verbal communication and presentation skills; ability to represent NVIDIA Inception as a technically credible platform partner * Curious, analytical, and proactive attitude with a continuous focus on improving technical enablement, platform adoption, and ecosystem outcomes * Willingness to travel around 40% of the time across Europe to engage directly with startups, developers, and investors **Ways To Stand Out From The Crowd** * Hands\-on experience working with or supporting companies building on CUDA libraries, NVIDIA SDKs, or GPU\-accelerated AI infrastructure * Prior experience at a top startup accelerator, data\-focused startup, developer\-platform organization, or AI infrastructure provider * Demonstrated ability to operate effectively in a highly collaborative, matrixed organization, aligning ecosystem needs with platform, product, and business priorities * Strong orientation toward metrics, analytics, and platform adoption measurement, with the ability to assess developer engagement, technical depth, and ecosystem impact NVIDIA is at the forefront of breakthroughs in Artificial Intelligence, High\-Performance Computing, and Visualization. Our teams are composed of driven, innovative professionals dedicated to pushing the boundaries of technology. We offer highly competitive salaries, an extensive benefits package, and a work environment that promotes diversity, inclusion, and flexibility. As an equal opportunity employer, we are committed to fostering a supportive and empowering workplace for all. , , JR2023583

Incubators & Accelerators

Lead Scientist - Bioanalysis

Labcorp

Harrogate, England, UK

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data\-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives. **Lead Scientist – LCMS** Our largest UK site in Harrogate, North Yorkshire is currently recruiting for a Lead Scientist to join the LCMS team. **Job Responsibilities Include** * Lead scientific activities supporting method development, validation, and sample analysis projects * Serve in key study leadership roles (e.g., Study Director, Principal Investigator, Responsible Scientist) for regulated and non\-regulated studies. * Develop, review, and approve protocols, validation plans, reports, and study data. * Provide scientific oversight to ensure compliance with GLP, GCP, regulatory, and client requirements. * Act as the primary scientific contact for clients, defining project requirements and managing scientific expectations. * Identify and resolve scientific challenges, risks, and scope changes throughout the study lifecycle. * Provide technical expertise and support assay troubleshooting and scientific investigations. * Lead, mentor, and develop scientific staff while fostering collaboration and a culture of quality. * Manage multiple complex projects, ensuring delivery to quality, timeline, and client expectations. * Drive continuous improvement initiatives that enhance scientific excellence and client satisfaction. **Minimum Qualifications** * Advanced scientific degree (or equivalent experience) in a relevant discipline. * Strong experience in bioanalytical method development, validation, and regulated study conduct. * Thorough understanding of GLP, GCP, and applicable regulatory requirements. * Proven ability to interpret complex scientific data and make sound technical decisions. * Excellent client management, communication, and stakeholder engagement skills. * Demonstrated leadership, mentoring, and project management experience. * Ability to manage a high\-volume workload while maintaining scientific quality and attention to detail. Are you looking for your next opportunity in Bioanalysis (LC\-MS/MS)? Are you at a stage in your career where you are ready to work on a variety of studies with differing levels of complexity? Do you want to be the pivotal point between our clients and scientists? Do you want to work for a world class leading company who work together to build a Healthier and Safer world? If this sounds like you, Labcorp is looking for a **Lead Scientist** to join our growing Bioanalysis (LC\-MS/MS) team in **Harrogate.** The Lead Scientist is responsible for the management of bioanalytical (LC\-MS/MS) studies/phases of studies and to ensure that all work is conducted in accordance with the Study Plan, SOPs and appropriate regulatory standards such as GLP \& GCP, and guidelines (EMA and FDA Bioanalytical Method Validation, SANTE etc.). To run on a day to day basis and report, studies of various types and complexity. We are looking for a strategic scientific leader with strong technical expertise, a customer\-focused mindset, and a passion for delivering high\-quality science while developing teams and building strong client partnerships. **Labcorp Is Proud To Be An Equal Opportunity Employer** Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

Pharma & Biotech

Medical Advisor

Johnson & Johnson Innovative Medicine

High Wycombe, England, UK

At Johnson \& Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson \& Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson \& Johnson, we respect the diversity and dignity of our employees and recognize their merit. **Job Function** Medical Affairs Group **Job Sub Function** Medical Affairs **Job Category** Scientific/Technology **All Job Posting Locations:** High Wycombe, Buckinghamshire, United Kingdom **Job Description** At Johnson \& Johnson, we are committed to addressing and solving some of the most meaningful unmet medical needs through creating an environment where our employees feel valued and can reach their potential. This commitment is embedded in our Credo! **We at Johnson \& Johnson are recruiting for a Medical Advisor \- Oncology, located in Maidenhead, UK** This role sits within Medical Affairs and focuses on medical science engagement, clinical research activities, and external collaborator teamwork. The position contributes to the execution of strategy and supports outcomes for patients and the healthcare community! The Medical Advisor is a key member of the cross\-functional Therapy Area team, providing high\-quality medical leadership, scientific expertise, and strategic input to support patient outcomes, Healthcare Professionals (HCPs), and the NHS. The role partners closely with Medical Affairs, Market Access, Commercial, HEOR, and Regulatory colleagues to develop and execute the local medical strategy **Key Responsibilities** * Build and maintain deep expertise in related therapy area in oncology, staying up to date with clinical and scientific advances through actively engaging with key clinicians and academics. * Gather and translate field insights to inform medical strategy and evidence generation * Contribute to local evidence generation strategy by identifying data gaps and proposing research initiatives * Contribute to the development and execution of the local Medical Affairs plan in related therapy areas * Lead or support key medical affairs projects (e.g., advisory boards, scientific exchange, medical education programmes) * Collaborate with Market Access colleagues providing medical expertise on Health Technology Appraisal submission(s) * Work closely with Commercial, Regulatory, and Global/EMEA teams to ensure aligned strategy and execution * Ensure all activities comply with ABPI Code of Practice and company policies * Act as medical reviewer/final signatory (if qualified), ensuring scientific accuracy and balance **Qualifications** * GMC registered physician or Pharmacist with UK registration * PhD in oncology, immunology, molecular biology, or related discipline * MSc with experience in Medical Affairs in pharmaceutical industry * Other relevant healthcare qualifications combined with substantial Medical Affairs experience **Required** **Experience and Skills:** * Strong project management skills and demonstrated experiences in leading clinical/ scientific programs with a high degree of autonomy * Good understanding of ABPI Code of Practice * Experience in evidence generation, data interpretation, and scientific communication * Ability to learn quickly, build and maintain relationships **Preferred** * Experience as a Medical Advisor in lung, colorectal, or head and neck cancer preferred * Experience supporting Health Technology Appraisal Submissions *Johnson \& Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.* *Johnson \& Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact\-us/careers, internal employees contact AskGS to be directed to your accommodation resource.* **Required Skills** **Preferred Skills:** Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Coaching, Collaboration, Communication, Critical Thinking, Data Analysis, Data Savvy, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Product Development Lifecycle, Report Writing, Stakeholder Engagement, Technologically Savvy

Public Health, Policy & Government

Clinical Program Leader

EPM Scientific

Surrey, England, UK

Key Responsibilities Clinical Program Leadership * Lead global and European clinical programs across a rare disease portfolio from planning through execution and study completion. * Drive program delivery, ensuring alignment with broader clinical development and corporate objectives. * Maintain oversight of timelines, budgets, quality metrics, risk management, and overall program performance. * Provide regular strategic updates and recommendations to senior leadership and governance committees. * Coordinate and lead cross\-functional teams across Clinical Operations, Medical Affairs, Regulatory Affairs, Biometrics, Drug Safety, and external partners. * Support the progression of rare disease indications through key development milestones and toward approval. Clinical Execution \& Delivery * Ensure operational excellence across all stages of clinical trial delivery. * Provide oversight of study conduct, patient safety, data integrity, and regulatory compliance. * Support protocol development and implementation of Quality by Design principles. * Review clinical data, study progress, and key performance indicators to drive informed decision\-making. * Lead study reporting activities, CSR development, and support regulatory submissions. * Maintain inspection readiness and oversee audit preparation and regulatory interactions. Cross\-Functional Leadership * Lead multidisciplinary project teams to deliver program objectives efficiently and effectively. * Foster strong collaboration between internal functions and external stakeholders. * Drive accountability and alignment across all program contributors. * Act as a key clinical representative during governance meetings and strategic planning discussions. * Build strong working relationships with investigators, KOLs, CROs, and vendors. Site \& Vendor Oversight * Oversee site feasibility, site selection, contracting, budgets, recruitment, and operational performance. * Lead vendor selection, governance, and performance management activities. * Ensure CROs and service providers deliver against agreed timelines and quality expectations. * Support investigator engagement, site training initiatives, and study\-related meetings. * Provide guidance and oversight to Clinical Study Leads and Clinical Project Associates. Leadership \& Team Development * Provide leadership, coaching, and mentorship across clinical teams. * Support resource planning and allocation across programs. * Develop team capabilities through training, knowledge sharing, and best practice initiatives. * Foster a culture of continuous improvement, collaboration, and operational excellence. * Contribute to the ongoing growth and development of the Clinical Affairs function. Innovation \& Continuous Improvement * Identify opportunities to enhance clinical trial execution and program efficiency. * Support implementation of innovative approaches, technologies, and digital solutions. * Drive process improvements across the clinical development organisation. * Contribute to external scientific and clinical communications where appropriate. * Represent the organisation at industry meetings, conferences, and regulatory interactions.

Research

Safety Investigation and Risk Manager

British Airways

Hounslow, England, UK

**A career without limits** As the nation’s flag carrier, we take great pride in connecting Britain with the world and the world with Britain. It’s something we’ve been doing for over 100 years, ever since we launched the world’s first international scheduled air service between London and Paris. This originality has been in our blood since day one. It’s the spirit we share with the people that fly with us, our partners, and our colleagues. So, whether you are a reassuring voice on the end of a phone, a smile at the door, under a wing keeping the turbines spinning or landing us gently in far\-flung places, a job at British Airways is yours to make. We know great things can happen when you’re inspired to think big and bring your ambition to work every day, which is why, at British Airways the sky is never the limit. **The Role** *Risk and Investigation Manager* *This is an exciting opportunity to join the British Airways Corporate Safety, Security and CAMO Directorate as an Investigation and Risk Manager. The role is instrumental in delivering the vision of world class risk management by proactively managing risk as well as performing complex effective investigations influencing change across the organisation.* **What You’ll Do** *The Risk Manager and Investigation plays a key role in maintaining and enhancing safety performance across British Airways. You will lead complex safety investigations, provide independent challenge and oversight, and support the identification, assessment and management of strategic and operational risks. Using a systems\-based approach, you will identify underlying causes, drive organisational learning and influence meaningful improvements to processes, controls and ways of working. Working closely with senior leaders and operational teams, you will provide expert advice, assurance and insight to support effective decision making, regulatory compliance and continual improvement across the business.* **What You’ll Bring To British Airways** * Good understanding of the principles involved with Safety investigations including system\-based thinking * Good understanding of aviation safety and security management systems, operational procedures and regulatory requirements within a complex, safety\-critical environment. * Strong influencing and communication skills. * Ability to work collaboratively across Directorates in a regulated environment. * Ability to lead a team in the investigation of incidents and accidents. * Working knowledge of UK, EU and US safety regulations. * Experience applying structured investigation methodologies and translating findings into effective corrective and preventative actions. * Experience using safety reporting, occurrence management and risk management systems. * Detailed knowledge and understanding of the principles of occupational and aviation safety management. * Ability to obtain and maintain airside identity card * Ability to obtain and maintain airside driving permit **Your Experience** * Recognised investigation course training (essential) * Recognised Health \& Safety qualification (desirable) * Recognised Human Factors qualification (desirable) * Experience in cross and multi\-functional working. * Experience working across departments and external organisations/regulators * Experience promoting and supporting a positive reporting culture, Just Culture principles and proactive safety management. * Participation in corporate response to accidents and serious incidents. **What We Offer** We believe that all the people who work with us should feel valued for the part they play. It’s one of the reasons our rewards go far beyond a competitive salary. From the day you join us, you’ll get access to brilliant staff travel benefits including unlimited basic and premium standby tickets on British Airways flights. You’ll also receive up to 30 discounted ‘Hotline’ airfares per year for yourself, friends, and family. At British Airways you’ll have the chance to take on new challenges and move forward in a way that feels right for you. We encourage all those who work for us to consider opportunities right across our business to help you develop and progress. We never stand still, and we don’t expect our people to either. **Inclusion \& Diversity** At British Airways we all have a part to play in creating an inclusive place to work. Diverse representation among our people is really important to us and we recognise that all our colleagues are uniquely different and bring their own originality, creativity and identity to work. Inclusion and diversity is a key driver of innovation and we’re committed to creating a culture where everyone feels that they can be themselves. We’re looking for people from all backgrounds and cultures to join us and be a part of our journey to become a Better BA as we continue to connect Britain with the world and the world with Britain.

Pharma & Biotech

Card disputes/chargeback Specialist

JPMorganChase

Edinburgh, Scotland, UK

**Job Description** Be the person customers trust when something does not look right on their card transaction. You will protect customer experience by investigating non\-fraud disputes and guiding cases through the chargeback process with care and confidence. Through phone and chat, you will bring empathy, clarity, and ownership to every interaction. As our business expands, you will join a team committed to raising service standards and doing the right thing for customers. As a Banking Operations Disputes Specialist in International Consumer Business, Banking Operations, you will support our customers by reviewing non\-fraud card disputes and managing chargebacks end\-to\-end with care, accuracy, and timely decisions. You will help us deliver a consistent, high\-quality customer experience across channels while strengthening our controls and documentation. You will also contribute to a collaborative environment by sharing knowledge and improving how we resolve disputes. **Job Responsibilities** * Review card transaction disputes to confirm validity and identify the appropriate resolution path. * Investigate customer concerns through thorough research and sound judgment to reach fair outcomes. * Process chargebacks accurately by completing required steps across the full chargeback lifecycle. * Communicate clearly and professionally with customers through phone and chat, setting expectations and guiding next steps. * Document case activity thoroughly and concisely while engaging with customers in real time. * Resolve complaints within agreed service timeframes, escalating when needed to meet customer and business outcomes. * Identify trends, gaps, or recurring issues and log them appropriately to support continuous improvement. * Support daily banking calls as needed to maintain coverage and service consistency. * Adhere to applicable regulatory requirements and departmental policies and procedures. **Required Qualifications, Capabilities, And Skills** * Willingness to work rotating schedules and shifts (business hours are 08:00 to 20:00, Monday to Sunday; four 10\-hour shifts per week; one weekend in eight, subject to change). * Willingness to work in an environment supporting customers through both phone and chat. * Strong customer focus, including ownership of interactions, empathy, and effective expectation\-setting. * Strong verbal and written communication skills, including negotiation and decision\-making with customers and internal partners. * Ability to multitask while speaking or chatting with customers and documenting account activity clearly. * Strong problem\-solving skills, including prioritization and timely decision\-making. * Strong analytical skills with attention to detail and accuracy. * Proficiency using multiple windows, browsers, tabs, and messaging tools. * Ability to follow regulatory requirements and internal policies and procedures. * Ability to produce clear, accurate case notes and supporting documentation. **Preferred Qualifications, Capabilities, And Skills** * Experience with chargeback rules and end\-to\-end chargeback processes. * Experience conducting investigations and reviews of credit card disputes (non\-fraud). \#ICBCareer \#ChaseUKCustomerServices **About Us** J.P. Morgan is a global leader in financial services, providing strategic advice and products to the world's most prominent corporations, governments, wealthy individuals and institutional investors. Our first\-class business in a first\-class way approach to serving clients drives everything we do. We strive to build trusted, long\-term partnerships to help our clients achieve their business objectives. We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. We do not discriminate on the basis of any protected attribute, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. We also make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as mental health or physical disability needs. Visit our FAQs for more information about requesting an accommodation. **About The Team** Our professionals in our Corporate Functions cover a diverse range of areas from finance and risk to human resources and marketing. Our corporate teams are an essential part of our company, ensuring that we're setting our businesses, clients, customers and employees up for success.

Medical Device

Dispute Resolutions Specialist

Oakley Recruitment Ltd

Coventry, England, UK

**Oakley Recruitment is working in partnership with an expanding organisation based in Coventry. This is an excellent opportunity to join the team as a Dispute Resolutions Executive on a full\-time permanent basis** **Culture and Environment** Our client offers a collaborative and fast\-paced environment where accuracy, accountability, and continuous improvement are highly valued. This is a business that encourages professional growth, cross\-functional collaboration, and proactive thinking, within a supportive hybrid working environment. **Personality** You’ll be a calm, confident and solutions\-focused individual who is comfortable managing challenging conversations and making fair, evidence\-based decisions. You’ll have a naturally customer\-focused approach while understanding the importance of protecting commercial interests and following contractual obligations. Highly organised and detail\-oriented, you’ll be confident managing multiple cases at once and taking ownership of disputes from initial review through to resolution. You’ll communicate clearly and professionally, work well with a variety of stakeholders and bring a high level of integrity and accountability to your work. A collaborative mindset and willingness to identify ways of improving processes will also be key to succeeding within the team. **Reward** * SAIP 8\.5% target paid annually * Private medical insurance * Role specific Car Ownership Scheme * 26 days’ annual leave plus paid bank holidays * Additional days leave to be taken in the month of your birthday * Holidays increase with service * Pension scheme 10% employer if you put in 5 * Life insurance subject to policy term * Group Income Protection (subject to policy terms) * Employee wellbeing \& assistance programme * Subsidised gym * Hybrid Working * Discounts with known Highstreet retailers via the Employee Benefits Hub * ‘Friends \& Family’ car discounts * Recognition awards and engagement initiatives across the organisation **Job Role:** * Managing end\-of\-lease disputes relating to vehicle condition, damage charges, excess mileage, missing items and early termination costs * Reviewing vehicle inspection reports, photographs, engineer assessments and contractual documentation to determine the validity of disputes * Making fair and evidence\-based decisions in line with contractual agreements and recognised industry standards * Communicating dispute outcomes clearly and professionally to customers, brokers and internal stakeholders * Acting as a point of escalation and subject\-matter expert for complex end\-of\-lease disputes * Handling sensitive and challenging customer cases with empathy, professionalism and clarity * Explaining technical vehicle assessments and contractual terms in a clear and customer\-friendly way * Ensuring dispute handling complies with relevant consumer legislation, FCA principles where applicable and internal policies * Maintaining accurate case records and audit trails to support internal reviews and external escalations * Supporting responses to cases referred to independent bodies, including BVRLA conciliation and the Financial Ombudsman Service where applicable * Liaising with inspection companies, auction partners, refurbishment providers, legal teams and finance colleagues to resolve cases * Tracking dispute volumes, outcomes, agreed write\-offs and recovery values * Identifying recurring dispute trends and root causes while recommending improvements to processes and policies * Supporting continuous improvement initiatives to enhance the end\-of\-lease customer journey * Contributing to training materials, FAQs and customer guidance relating to end\-of\-lease responsibilities **Skills and experience:** * Having a minimum of 3 years’ experience within a customer resolutions, disputes or complaints environment * Demonstrating experience within end\-of\-lease, vehicle inspections, contract hire operations or dispute and complaints handling * Understanding contract hire, vehicle leasing and end\-of\-lease processes * Having working knowledge of BVRLA Fair Wear \& Tear Standards * Interpreting contracts, vehicle inspection reports, photographs and damage assessments confidently * Demonstrating excellent attention to detail and making fair, evidence\-based decisions * Communicating confidently and professionally with customers and stakeholders both verbally and in writing * Managing conflict and handling complex or challenging customer conversations effectively * Organising and prioritising multiple cases while working to required timescales * Demonstrating strong commercial awareness while maintaining a fair and customer\-focused approach * Using case management systems and Microsoft Office applications confidently * Having experience within an FCA\-regulated environment, Ombudsman or independent conciliation processes being advantageous * Bringing previous automotive experience within leasing, fleet, remarketing or accident management being advantageous **Please Note: We do not contact or write to unsuccessful candidates. If we have not contacted you within 48 hours of your application, you should presume that your application was unsuccessful. By applying for this vacancy, you are permitting for Oakley Recruitment to contact you and retain your details. In compliance with the regulations (April 2004\) in place under the Employment Agencies Act, Oakley Recruitment will require proof of identification. A copy of your passport, birth certificate and NI number will be required, as part of your interview process.**

Medical Device

Complaint Handler

Vanguard

Manchester, England, UK

As a Complaint Handler, you will play a critical role in ensuring fair and professional resolution of client complaints within a regulated financial services environment. You will be responsible for managing the end\-to\-end complaints process, from initial investigation through to final response, while maintaining compliance with FCA, DISP, and other relevant regulatory frameworks. As a Complaint Handler, you will play a critical role in ensuring fair and professional resolution of client complaints within a regulated financial services environment. You will be responsible for managing the end\-to\-end complaints process, from initial investigation through to final response, while maintaining compliance with FCA, DISP, and other relevant regulatory frameworks. **What you’ll do:** **Investigate and Respond to Client Complaints:** * Manage end\-to\-end client complaints, acting as the primary point of contact throughout the process * Conduct thorough investigations by gathering and analysing evidence, reviewing client interactions, and liaising with internal teams * Communicate with clients in a clear, empathetic, and professional manner, keeping them informed of progress * Produce high\-quality Final Response Letters (FRLs), clearly outlining decisions and any remedial actions * Ensure all complaints are handled in line with FCA, DISP, and other regulatory requirements * Maintain accurate and comprehensive records for all cases **Process Adherence and Regulatory Compliance:** * Follow standardised complaints handling procedures, ensuring all actions comply with FCA, DISP, and other relevant regulations. * Ensure detailed and accurate record keeping. **Knowledge and Professional Development:** * Maintain up\-to\-date knowledge of financial products, complaint handling regulations, and best practices. * Demonstrate strong written and verbal communication skills, attention to detail, and sound judgment in all interactions. **What We’re Looking For** * Previous experience handling complaints within a regulated financial services environment * Strong understanding of FCA, DISP, and relevant regulatory frameworks * Excellent written and verbal communication skills * Strong analytical skills with the ability to make fair and balanced decisions * High attention to detail and the ability to manage complex or sensitive cases with professionalism and discretion * A collaborative, team\-oriented attitude and commitment to continuous improvement **Why join us?** * Be part of a supportive and collaborative team * Work in a role where you can make a real difference to customer outcomes * Gain exposure to a regulated environment with opportunities for professional development **Additional Information** * This role operates on a hybrid working model, with Tuesday to Thursday based in the office * Please note that Vanguard is unable to offer visa sponsorship for this position **How We Work** Vanguard has implemented a hybrid working model for the majority of our crew members, designed to capture the benefits of enhanced flexibility while enabling in\-person learning, collaboration, and connection. We believe our mission\-driven and highly collaborative culture is a critical enabler to support long\-term client outcomes and enrich the employee experience.

Medical Device

Validation Engineer - Medical Devices

MEDASIL SURGICAL LIMITED

Leeds, England, UK

**Validation Engineer \- Medical devices** **Medasil Surgical Ltd** **Leeds \| Full Time \| Permanent \| On\-site** **Working Hours:** Monday: 8:00am–4:30pm Tuesday–Thursday: 7:30am–4:30pm Friday: 7:30am–2:00pm **About Medasil Surgical Ltd** Medasil Surgical Ltd is a specialist medical device manufacturer based in Leeds. We manufacture medical devices within a regulated environment, with quality and compliance central to our manufacturing operations. We are seeking a **Validation Engineer** to join our Technical and Engineering team. **The Role** The Validation Engineer will be responsible for the planning, execution, documentation and maintenance of validation and verification activities across the company’s manufacturing operations. The role covers the validation and verification of **manufacturing equipment, processes, tooling, test methods, software, facilities and associated systems** used in the manufacture of medical devices. The Validation Engineer will work closely with Engineering, Production, Quality Assurance, Regulatory Affairs and other relevant departments to ensure that equipment, processes and systems are appropriately qualified and remain in a validated state throughout their lifecycle. **Key Responsibilities** * Plan, develop and execute validation and verification activities in accordance with approved procedures, validation plans and the company’s Quality Management System. * Prepare and execute **(IQ), (OQ) and (PQ)** protocols and reports. * Develop validation strategies, protocols, test methods, acceptance criteria and sampling plans. * Validate and qualify manufacturing equipment, tooling and associated processes. * Work with equipment and processes including **injection moulding, extrusion, compression moulding, ovens, washing, assembly, sealing and inspection/test equipment** . * Support the preparation and review of Process FMEAs and other risk assessments. * Identify Critical Process Parameters (CPPs), Critical Quality Attributes (CQAs) and other characteristics requiring control or verification. * Provide validation input into engineering and quality change controls and determine requirements for qualification, verification or revalidation. * Support the introduction and qualification of new equipment, processes, tooling, software and manufacturing technologies. * Maintain accurate, complete and traceable validation documentation and records. * Support internal, customer, Notified Body and regulatory audits relating to validation and engineering activities. * Assist with the preparation and maintenance of the Site Validation Master Plan, validation schedules and validation status documentation. * Identify opportunities for improvement in validation processes, manufacturing processes and equipment performance. **Experience and Knowledge** **Skills and Attributes** The role requires: * Strong analytical and problem\-solving skills. * Excellent attention to detail. * The ability to investigate technical problems and identify appropriate root causes. * Excellent written and verbal communication skills. * The ability to write clear validation protocols, reports, risk assessments and technical documentation. * Good understanding of data analysis and the ability to interpret validation and process performance data. * The ability to work independently and as part of a cross\-functional team. * Good time management and organisational skills. * The ability to manage multiple validation activities and meet agreed deadlines. * The ability to adapt to changing priorities and work effectively under time constraints. * The ability to maintain accurate and traceable validation records. * The ability to communicate effectively with Engineering, Production, Quality, Regulatory Affairs, suppliers and external contractors. * The confidence to challenge processes, assumptions and technical conclusions where appropriate and provide evidence\-based recommendations. * Good working knowledge of Microsoft Word and Excel, including using Excel for validation data analysis. * The ability to work on the manufacturing floor and within controlled/cleanroom environments where required. **Working at Medasil** The Validation Engineer will work as part of the Technical and Engineering team and will have regular interaction with Engineering, Production, Quality Assurance and Regulatory Affairs. The role involves both office\-based technical and documentation work and practical activity within the manufacturing environment. The successful candidate will be expected to work independently on assigned validation projects while maintaining effective communication with relevant teams. **Application** To apply for this position, please submit your CV and a covering letter outlining your relevant experience in validation, engineering and/or regulated manufacturing.

Medical Device

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