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Part-Time Study Start-Up Lead, UK Clinical Trials
Job summary
A leading global Contract Research Organization is seeking an experienced Study Start-Up Lead to oversee study start-up activities within the Internal Medicine and Neuroscience business unit on a part-time (0.4 FTE) basis. You will lead compliance efforts and manage timelines while collaborating with cross-functional teams to ensure regulatory readiness. Ideal candidates will possess solid experience in CRO or pharmaceutical environments and knowledge of UK submission processes. Join a team dedicated to making a difference in patient lives.
Benefits
Qualifications
- Proven experience in study start-up within a CRO or pharmaceutical environment.
- Strong knowledge of UK regulatory and ethics submission processes.
- Experience in Internal Medicine and/or Neuroscience studies is highly advantageous.
Responsibilities
- Lead and oversee all study start-up activities for assigned projects.
- Coordinate submissions to ethics committees and Regulatory Authorities.
- Ensure compliance with ICH-GCP and local regulations.
Skills
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.