Senior Medical Director, Oncology Early Development

Role: Senior Medical Director overseeing early-phase clinical development programs, primarily in oncology, with responsibilities spanning trial design, regulatory compliance, data interpretation, and cross-functional collaboration. Responsibilities include managing clinical trial execution, ensuring data integrity, overseeing safety and efficacy assessments, and contributing to regulatory submissions and scientific documentation. The role may involve leading Clinical Strategy Teams, engaging with external thought leaders, and supporting business development activities. Qualifications: MD or DO with at least 3 years of clinical trial experience, including 2+ years in the pharmaceutical industry; expertise in oncology, especially thoracic malignancies and T-cell engagers, preferred. Essential skills include clinical trial methodology, regulatory knowledge, and experience with PK/PD modeling. The role requires strong communication skills and the ability to lead cross-functional teams. High-Value: Oncology (thoracic malignancies, T-cell engagers), early-phase trials, global drug development, regulatory compliance, GxP adherence, and cross-functional leadership. Work setup and travel details are not specified.