London, UK (Hybrid) Full Time, Permanent
We are looking for a motivated Clinical Research Associate (CRA) who is detail oriented to join a growing research team. This hybrid role requires the candidate to monitor clinical trial sites within a reduced travel area in London and maintain close engagement with investigative sites. The successful candidate will ensure that all clinical studies are conducted in line with ICH‑GCP, applicable regulations, study protocols and sponsor requirements. You will have to work well together with investigators, staff, and internal project teams to support the successful delivery of clinical trials.
Key Responsibilities
- Make sure the clinical trial data is accurate, complete and integral.
- Protocol deviations and outstanding site issues must be identified, documented and checked up on.
- Build and maintain strong working relationships with the site personnel and investigators.
- Support site training and provide constant guidance throughout the study life cycle.
- Prepare monitoring reports and sustain essential trial documentation.
- To ensure study milestones are completed, the candidate will need to work with Clinical Trial Managers and cross-functioned teams.
- Help support regulatory audits and inspection readiness where required.
- Maintain accurate tracking of site performance and recruitment.
Essential Requirements
- Bachelor’s degree in Life Sciences
- Minimum 2 years’ experience working as Clinical Research associate in clinical research
- Strong organisational skills with exceptional attention to detail
- Full right to work in the UK
Desirable
- Having experience in multiple therapeutic areas.
- Experience in working in a CRO, sponsor or academic clinical research environment.
What we offer
- Competitive salary
- Opportunities for career progression.
- Pension scheme and annual leave entitlement.
Working Pattern
- Hybrid Work
- All sites within London.
CLINICAL RESEARCH ASSOCIATE (CRA) employer: Barrington James
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