Job Summary

• Co-chairs clinical study teams and provides clinical and scientific expertise to strategy and protocol development.
• Designs and writes clinical trial outlines, protocols, and amendments, ensuring consistency with objectives and minimizing amendments.
• Oversees study team work, contributes to vendor selection, and ensures regulatory compliance for clinical trials and reporting.

Matching Summary

Skills & Requirements

Key Requirements

• M.D., Ph.D., D.V.M., M.S., and/or PharmD or equivalent qualifications
• Postgraduate training, certification or fellowship in a medical discipline or drug development is preferred
• Demonstrated scientific productivity
• Thorough understanding of local and international regulations
• Practical experience in clinical trial strategies, methods and processes
• Track record of design, oversight and interpretation of clinical studies
• Previous leadership or management experience or training
• Knowledge and experience in Good Clinical Practices (GCP)
• Experience in conduct and execution of clinical trials

Work Rights