Medical Director

The Medical Director provides hands‑on medical monitoring and clinical expertise to support the design, conduct, and interpretation of clinical trials. This role is responsible for ensuring subject safety, data integrity, and protocol compliance in accordance with ICH‑GCP and applicable regulatory requirements.

Key Accountabilities

• Study‑Level Medical Monitoring (Primary Responsibility)
  • Serve as the primary Medical Monitor for assigned clinical trials.
  • Act as the first point of contact for investigative sites for medical questions related to eligibility, enrollment, and patient management.
  • Provide timely medical guidance on protocol‑related questions, including inclusion/exclusion criteria and subject eligibility.
  • Be available to address medical questions and issues arising during study conduct, including urgent safety matters.
• Safety Review & Signal Detection
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