What You'll Do

Lead Local Study Team(s) at country level to deliver clinical studies according to resources, budget, and timelines. Ensure site qualifications, setup, initiation, monitoring, and closure are performed. Coordinate site selection and ensure timely submission of documents to EC/IRB and Regulatory Authority.

What We're Looking For

Experience in clinical study management and site monitoring. Strong knowledge of ICH-GCP and local regulations. Proven ability to lead teams and manage study budgets effectively.

Additional Information

Experience Level

Senior

Job Language

English

Employment Type

Full-time

Work Mode

Remote