About the job
Key Responsibilities Act as Principal Investigator or Sub-Investigator across a portfolio of clinical trials. Conduct medical assessments and ensure participant safety throughout study participation. Review eligibility criteria, medical histories, laboratory data, and adverse events. Support study feasibility, start-up activities, and sponsor engagement. Ensure all studies are conducted in accordance with ICH-GCP, protocol requirements, and regulatory standards. Provide medical oversight to res…
This is the summary supplied by Adzuna. See the full advert and salary details on Adzuna.