Clinical Development Medical Director (MD required)

Role: The Clinician Medical Monitor provides medical and scientific oversight for clinical trials, ensuring patient safety, study compliance, and data integrity. Responsibilities include designing study strategies, reviewing safety and efficacy data, advising on protocol development, and supporting regulatory interactions. The role involves participating in safety review teams, liaising with investigators and key opinion leaders, and contributing to regulatory documents and publications. Qualifications: MD/D.O. with at least 4 years of clinical experience, licensed to prescribe medicines, with a solid background in clinical research, regulatory processes, and safety monitoring. Preferred: experience in infectious diseases, clinical trials, and statistical knowledge. High-Value: Focus on clinical development, safety oversight, and protocol design within biopharma, with responsibilities encompassing pharmacovigilance, regulatory support, and collaboration with study teams. Work setup: Hybrid role, requiring onsite presence ~2.5 days/week in the U.S., with travel; salary range $239,900–$399,800, plus performance bonuses and benefits.