Medical Director / Senior Medical Director, Clinical Development

Role: Medical Monitor for late-stage development of varegacestat, focusing on desmoid tumors, providing medical oversight for global clinical trials. Responsibilities: oversee patient safety, review safety and efficacy data, evaluate adverse events, support protocol development, engage with investigators and external stakeholders, and contribute to regulatory submissions. Collaborate closely with Clinical Operations, Biostatistics, Regulatory Affairs, and other functions to ensure study integrity and compliance. Qualifications: MD or DO with 3+ years of industry clinical development experience, preferably in oncology, hematology, or internal medicine; board certification or specialized training; experience serving as Medical Monitor in interventional trials; strong knowledge of GCP, ICH guidelines, and global regulations. High-Value: Oncology (desmoid tumors), Phase 2/3 studies, rare diseases, regulatory support, global trial oversight, cross-functional collaboration. Work Setup: Not specified but implies a role supporting global clinical research, with an emphasis on medical oversight and strategic input.