CRC Level 1

JR159011 CRC Level 1

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a CRC Level 1 to join our team at our Warwickshire clinical research site. This is a fully site-based role and an excellent opportunity for a healthcare professional looking to develop a career in clinical research while continuing to work directly with patients.

As a CRC Level 1, you will play an important role in the day-to-day delivery of clinical trials, supporting participants throughout their study journey and ensuring studies are conducted safely, accurately and in line with protocol requirements. We are particularly interested in candidates with hands-on clinical experience who are comfortable working directly with patients, performing clinical assessments and handling study-related documentation and data.

What you will be doing

• Supporting the delivery and coordination of clinical trial activities.
• Recruiting, screening and enrolling study participants.
• Conducting participant visits and supporting patients throughout the clinical trial process.
• Performing protocol-required clinical procedures, including:

• Phlebotomy and sample processing
• Vital signs assessments
• ECGs and other study-specific procedures
• Collection and documentation of clinical data

• Maintaining accurate source documentation and study records.
• Entering study data into Electronic Data Capture (EDC) systems and resolving data queries.
• Supporting study start-up activities, participant recruitment and retention efforts.
• Maintaining regulatory documentation and ensuring compliance with study protocols and SOPs.
• Working closely with Investigators, sponsors and monitors to support successful study delivery.
• Supporting monitoring visits, audits and inspection readiness activities.
• Educating participants about study requirements and the clinical trial process.
• Assisting with participant reimbursement and study administration activities.

Your Profile

• Qualification in Nursing, Biomedical Science, Healthcare Science, Life Sciences or another relevant healthcare discipline.
• Previous healthcare experience involving direct patient contact is highly desirable.
• Experience with phlebotomy, sample handling, clinical observations or other patient-facing clinical procedures would be advantageous.
• Strong attention to detail and excellent documentation skills.
• Comfortable working with both patients and clinical data.
• Good organisational skills and the ability to manage multiple tasks effectively.
• Strong communication and interpersonal skills.
• Proficiency in Microsoft Office applications and confidence working with electronic systems.
• An interest in clinical research and developing a career within the clinical trials industry.

Why Join Us?

This is a fantastic opportunity to join a growing clinical research team and contribute to the development of new medicines and treatments. You'll gain hands-on experience across a variety of clinical studies while working in a supportive environment where patient care and research excellence go hand in hand.

• Please note: This is a fully office/site-based role in Warwickshire. Candidates should be comfortable with regular patient interaction, phlebotomy, clinical procedures, laboratory sample handling and clinical data entry.

What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion &​ belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply