At a Glance
- Tasks: Coordinate regulatory submissions and ensure compliance for early-phase clinical trials.
- Company: Fortrea, a leader in clinical research with a focus on innovation.
- Benefits: Dynamic work environment, professional growth, and the chance to impact healthcare.
- Other info: Opportunity to contribute to both UK and US submissions.
- Why this job: Join a team making a difference in clinical trials and develop your regulatory expertise.
- Qualifications: Relevant degree and 2 years of experience in clinical research required.
The predicted salary is between 30000 - 40000 £ per year.
Fortrea is seeking a UK-based Site Start‑Up Specialist to support early-phase clinical trials. The role involves coordinating regulatory submissions and working closely with investigative sites to ensure compliance with ICH regulations.
Candidates need a relevant degree and 2 years of experience in clinical research. This position offers a dynamic work environment, contributing to both UK and US submissions while developing expertise in regulatory processes.
UK Site Start-Up Specialist for Clinical Trials employer: Fortrea
Fortrea is an exceptional employer, offering a vibrant work culture that fosters collaboration and innovation in the field of clinical research. With a strong emphasis on employee growth, team members benefit from ongoing training and development opportunities while contributing to impactful early-phase clinical trials. Located in the UK, our dynamic environment allows for meaningful contributions to both UK and US regulatory submissions, making it an ideal place for professionals seeking rewarding careers in healthcare.
