At a Glance
- Tasks: Facilitate the start-up of early-phase clinical trials and manage regulatory submissions.
- Company: Fortrea, a leader in clinical research with a collaborative culture.
- Benefits: Gain expertise in UK regulatory processes and enjoy a dynamic work environment.
- Other info: Join a team that values collaboration and offers growth opportunities.
- Why this job: Make a real impact in clinical trials while developing your career in research.
- Qualifications: Experience in clinical research and strong communication skills required.
The predicted salary is between 35000 - 45000 £ per year.
Fortrea is seeking a Site Start-Up Specialist based in the UK to facilitate the start-up of early-phase clinical trials. The ideal candidate will manage regulatory submissions, coordinate with investigative sites, and ensure compliance with guidelines and standards.
This position offers an opportunity to develop expertise in UK regulatory processes while working in a dynamic and collaborative environment.
Previous experience in clinical research is essential, alongside strong communication skills and a solid understanding of regulatory frameworks.
UK Site Start-Up Specialist for Clinical Trials in Leeds employer: Fortrea
Fortrea is an exceptional employer that fosters a dynamic and collaborative work culture, perfect for those passionate about advancing clinical research. Employees benefit from comprehensive training in UK regulatory processes, ample opportunities for professional growth, and a supportive environment that values innovation and teamwork. Joining Fortrea means being part of a mission-driven organisation dedicated to making a meaningful impact in the field of clinical trials.
