Clinical Research Associate (CRA)
About the Role
We are seeking a motivated and detail-oriented Junior Clinical Research Associate (CRA) to join our team. This is an excellent opportunity for someone with at least one year of on-site monitoring experience, ideally gained within a CRO environment. The successful candidate will be responsible for monitoring clinical trials to ensure compliance with regulatory requirements, Good Clinical Practice (GCP), and study protocols.
Key Responsibilities
- Conduct on-site and remote monitoring visits to ensure compliance with study protocols, GCP, and regulatory requirements.
- Perform source data verification and ensure data accuracy and completeness.
- Build and maintain strong relationships with site staff to support study conduct and patient recruitment.
- Identify and resolve site-level issues, escalating as needed.
- Prepare and submit monitoring visit reports and follow-up documentation in a timely manner.
- Collaborate with internal teams to support study timelines and deliverables.
Requirements
- Minimum 1 year of independent monitoring experience in a clinical research setting.
- Experience working within a CRO or similar environment is acceptable.
- Strong understanding of ICH-GCP and clinical trial regulations.
- Excellent communication, organizational, and problem-solving skills.
- Ability to work independently and manage multiple priorities.
- Must be UK-based and able to work on-site in West London 2 days per week.
- Willingness to travel for site visits as required.
Preferred Qualifications
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Experience across multiple therapeutic areas is welcome but not essential.
Why Join Us?
- Competitive compensation and benefits package.
- Work with a collaborative, mission-driven team.
- Opportunities for professional development and internal growth.
- Contribute directly to the development of life-changing therapies.
FAQs
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