Senior Medical Director, Oncology Early Development

Role: Senior Medical Director leading early-phase clinical development programs in immunology, oncology, or neuroscience, with a focus on designing, executing, and interpreting clinical trials. Responsibilities: oversee study design, ensure study integrity, monitor safety and efficacy, and lead cross-functional teams; develop and review protocols, regulatory submissions, and scientific reports; serve as a clinical expert, contribute to strategic planning via Clinical Strategy Teams, and liaise with external opinion leaders. Qualifications: MD or DO with at least 3 years of clinical trial experience, including 2+ years in the pharma industry; strong expertise in clinical research methodology, regulatory standards, and GxP; experience in thoracic malignancies or T-cell engagers preferred; excellent communication skills in English. High-Value: early-phase (likely Phases 1/2) clinical trials, biologics or small molecules, primarily in immunology, oncology, or neuroscience; regulatory compliance, pharmacovigilance, and study oversight; global clinical development involvement. Collaboration: cross-functional engagement with Medical Affairs, Discovery, Regulatory, and Commercial functions. WorkSetup: not specified; travel requirements not stated.