Senior Medical Director

📋 Description

• Deliver hands-on medical monitoring and clinical expertise to aid in the design, execution, and analysis of clinical trials.

• Ensure the safety of subjects, the integrity of data, and adherence to protocols in line with ICH-GCP standards.

• Serve as the primary Medical Monitor for designated studies.

• Act as a vital medical liaison for investigative sites and sponsors.

• Offer real-time medical advice and assess safety data.

• Participate in clinical and scientific discussions to facilitate high-quality study implementation.

⛳️ Requirements

• Doctor of Medicine (MD) from a recognized institution.

• A solid foundation in clinical medicine with hands-on experience in medical research or clinical development.

• At least 15+ years of experience in clinical development.

• Previous experience as a Medical Monitor in Phase I–IV clinical trials.

• Extensive knowledge of clinical trial methodology, safety evaluations, and medical data analysis.

• Familiarity with ICH-GCP, FDA, EMA, and other global regulatory frameworks.

• Preferred therapeutic expertise in oncology, hematology, or related disciplines.

• Experience in protocol development and clinical study design is preferred.

• Excellent communication skills, clinical judgment, and decision-making abilities.

• Exceptional attention to detail and capacity to manage multiple priorities.

• Experience in global, multi-regional clinical trials is preferred.

🏝️ Benefits

• Medical, dental, and vision coverage.

• Life and AD&D insurance.

• Short- and long-term disability benefits.

• Tuition reimbursement program.

• Fitness reimbursement.

• Employee assistance program (EAP).

• A 401(k)/pension plan.

• Generous paid time off.

• Sick leave.

• Opportunity to receive a performance-based bonus.