Medical Monitor

About the role

The Medical Monitor will oversee the safety and medical aspects of assigned clinical trials, providing continuous medical support and expertise to the project team and site investigators.

Key responsibilities

• Act as the primary medical monitor for designated clinical trials, offering 24/7 medical support.
• Interact with site investigators to share product information and assess medical and safety issues.
• Serve as the medical consultant to the project team, delivering therapeutic area expertise.
• Participate in data review, interpretation, and safety event processing.
• Provide protocol‑specific training to clinical site staff and other trial participants.
• Contribute medical input to study protocol design and final study reports.
• Attend and present at kick‑off meetings, investigator meetings, weekly team meetings, and client meetings as required.
• Maintain up‑to‑date knowledge of Good Clinical Practice (GCP) and regulatory requirements to ensure compliance.
• Mentor junior medical staff and demonstrate high ethical standards.

Required profile

• Basic medical degree (MD, MBBS, or equivalent).
• At least 2 years of experience in clinical research.
• Excellent interpersonal and communication abilities.
• Strong planning, organizational, and decision‑making skills.
• Team‑player with collaborative mindset.
• Meticulous analytical and scientific approach.
• Results‑oriented with a sense of urgency.
• High integrity, ethical conduct, and professionalism.
• Independent, self‑driven, and capable of driving change.
• Experience in coaching or mentoring is a plus.

Required skills

• Good Clinical Practice (GCP) knowledge.
• Familiarity with regulatory requirements for clinical development and safety.