When our values align, there's no limit to what we can achieve.
 

Are you passionate about advancing clinical research and making a real difference in patients' lives? Parexel is seeking an experienced Senior Clinical Study Administrator to join our FSP Clinical Operations team (fully outsourced to work for one of the largest Pharmaceutical company) and play a specialized role that bridges clinical administration with regulatory expertise, supporting ongoing studies with a focus on regulatory compliance and documentation excellence.

This is a remote position for candidates based in Istanbul or Ankara.

Key Responsibilities:
Regulatory Submissions & Maintenance: Lead and manage ongoing regulatory submissions and maintenance activities. Prepare, review, and track regulatory documents for submission to Ethics Committees, IRBs, and Regulatory Authorities. Ensure timely and compliant submission of all required documentation.
Inves...