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.
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