Clinical Development Medical Director (MD required)

Role: The Clinician Medical Monitor provides medical and scientific oversight for clinical trials, ensuring patient safety and study integrity across design, monitoring, and reporting. Responsibilities include safety assessment, review of adverse events, contributing to protocol development, supporting trial conduct, and liaising with regulatory bodies and investigators. They also participate in safety review teams and contribute to regulatory documents and publications. Requirements: Medical degree (MD/D.O.), 4+ years of relevant experience, licensure for independent prescribing, and experience in clinical research or pharmaceutical settings. Preferred: knowledge of statistics, infectious diseases, and trial management. High-Value: Focus on clinical trials in biopharma, likely post-IND, with responsibilities spanning safety monitoring, protocol input, and regulatory interactions. Work environment: Hybrid role based in the U.S., with occasional travel, requiring on-site presence approximately 2.5 days/week.