At a Glance
- Tasks: Administer clinical trials, coordinate participant recruitment, and ensure compliance with regulations.
- Company: CyDen, a leading organisation in clinical research based in Swansea.
- Benefits: Gain valuable experience in clinical research and develop your professional skills.
- Other info: This role is tailored for female candidates due to its specific nature.
- Why this job: Make a difference in healthcare while working in a dynamic and supportive environment.
- Qualifications: 1-3 years of clinical research experience and strong problem-solving skills required.
The predicted salary is between 30000 - 40000 £ per year.
<p>Cy Den 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.</p><p>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.</p> #J-18808-Ljbffr
Clinical Trials Coordinator: Data and Compliance in Swansea employer: CyDen
CyDen is an exceptional employer located in Swansea, offering a dynamic work environment that fosters collaboration and innovation in clinical research. With a strong commitment to employee development, we provide ample opportunities for growth and advancement, alongside a supportive culture that values diversity and inclusion. Our focus on maintaining high standards of compliance and data integrity ensures that our team members are engaged in meaningful work that contributes to the advancement of healthcare.
