Medical Director, Study Responsible Physician - Late Development, Prostate

Role: Director of Clinical Research Oncology supporting global oncology development programs, with a focus on developing and advancing cancer therapeutics. Responsibilities include leading cross-functional teams, overseeing clinical study design, start-up, execution, and data review, and ensuring regulatory compliance. The role involves collaboration with Data Management, Biostatistics, Regulatory Affairs, and external investigators, as well as mentoring study teams and contributing to regulatory submissions and scientific publications. Qualifications: MD or equivalent with at least 3 years of relevant oncology/uro-oncology clinical research experience, post-doctoral fellowship, and knowledge of cancer research and drug development. Preferred skills include clinical trial expertise, regulatory knowledge, stakeholder management, and strategic thinking. High-value specifics encompass oncology therapeutic area, late-stage (Phases 2-3) clinical trials, international study oversight, and matrix team leadership. The role requires up to 20-30% travel and offers a competitive salary range, with benefits aligned with corporate policies.