
Medical Director
Posted May 2

Posted May 2
• Deliver hands-on medical monitoring and clinical expertise to aid in the design, execution, and analysis of clinical trials.
• Ensure the safety of participants, maintain data integrity, and uphold protocol compliance.
• Act as the primary Medical Monitor for designated studies, offering real-time medical advice.
• Evaluate safety data and engage in clinical discussions.
• Collaborate effectively with Clinical Operations, Data Management, Biostatistics, and Pharmacovigilance.
• Doctor of Medicine (MD) from a recognized institution.
• At least 10+ years of experience in clinical development.
• Extensive experience in medical monitoring and oversight of clinical trials.
• Previous experience as a Medical Monitor in Phase I–IV clinical trials.
• Strong understanding of clinical trial methodologies, safety evaluations, and medical data analysis.
• Familiarity with ICH-GCP, FDA, EMA, and international regulatory standards.
• Preferred experience in contributing to protocol development and clinical study design.
• Medical, dental, and vision insurance.
• Life and AD&D insurance.
• Short- and long-term disability coverage.
• Tuition reimbursement program.
• Fitness reimbursement.
• Employee assistance program (EAP).
• 401(k)/pension plan.
• Generous paid time off and sick leave.
• Opportunity to earn a performance-based bonus.
Synchrony Group, LLC
Pfizer
Syneos Health
Thermo Fisher Scientific
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