Clinical Trials Coordinator: Data and Compliance

CyDen in Swansea seeks a candidate for a role involving the administration of clinical trials, coordinating participant recruitment, and ensuring compliance with regulatory standards. The successful applicant will need to manage trial documentation and maintain data accuracy while upholding Good Clinical Practice.

Ideal candidates will have 1–3 years of experience in clinical research, with strong problem-solving skills and a professional demeanor, along with a commitment to confidentiality. This position is tailored for female candidates due to the nature of the role.