Senior Medical Director, Oncology Early Development

Role: Senior Medical Director leading early-phase clinical development programs, primarily in oncology, with a focus on thoracic malignancies and T-cell engagers. Responsibilities include designing and overseeing clinical trials, ensuring data integrity, safety monitoring, and regulatory compliance; contributing to scientific documentation such as protocols, regulatory submissions, and study reports; and leading cross-functional teams and clinical strategy development. The role involves partnering with internal stakeholders, engaging with opinion leaders, and maintaining knowledge of therapeutic advancements to inform clinical plans. Qualifications: MD or DO with at least 3 years of clinical trial experience, including 2+ years in industry; strong expertise in clinical trial methodology, regulatory standards, and drug development, particularly in oncology. Preferred: experience with PK/PD modeling, translational strategies, and global trial management. HighValue: oncology, thoracic malignancies, T-cell engagers, early-phase (Ph1/Ph2), regulatory compliance, cross-functional collaboration, global trial oversight. WorkSetup: not specified.