Job Description
Clinical Research Associate
Location: Reading, Berkshire, UK
Work Setting: Site-based / UK travel
Employment Type: Full-time
Industry: Clinical Research / Life Sciences
Function: Clinical Operations / Research
About the Role
Seeking a Clinical Research Associate to support Oncology clinical trials across UK sites. The role involves independent site monitoring, study compliance, recruitment oversight and collaboration with clinical study teams.
Key Responsibilities
- Conduct site selection, initiation, monitoring and close-out visits in line with GCP.
- Support site recruitment plans and study delivery.
- Provide protocol and study training to assigned sites.
- Monitor site quality, protocol compliance and regulatory requirements.
- Track submissions, approvals, recruitment, CRF completion and data queries.
- Maintain TMF/ISF documentation and ensure accurate study records.
- Document monitoring findings, action plans and follow-up activities.
- Collaborate with study teams and site personnel to resolve issues.
Requirements
- Independent on-site monitoring experience within Oncology , particularly unblinded studies.
- Strong knowledge of GCP and ICH guidelines .
- Life science degree or equivalent clinical research industry experience.
- Willingness and flexibility to travel to UK study sites.
- Visa sponsorship is not available.
Interested in this role?
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