Medical Director, Study Responsible Physician - Late Development, Prostate

Role: Director of Clinical Research Oncology responsible for leading and executing global oncology clinical trials within a matrix team. Main objectives include delivering high-quality clinical studies, ensuring strategic and flawless study execution, and supporting regulatory submissions. Responsibilities encompass study planning, protocol development, medical review, investigator engagement, vendor oversight, and collaboration with cross-functional teams such as Data Management, Biostatistics, Regulatory, and GCO. The role involves mentoring study teams, managing study start-up activities, and contributing to scientific publications and regulatory interactions. Qualifications required are an M.D. or equivalent, with board certification or eligibility in Uro-Oncology or Oncology preferred, plus at least 3 years of relevant clinical research experience in cancer. Essential skills include strong scientific knowledge in oncology, clinical trial design, and stakeholder management, along with excellent communication. Experience with international, late-phase oncology trials in areas like solid tumors or hematologic malignancies is high-value. The position reports to a Clinical Leader, involves up to 20-30% travel, and is based in various U.S. locations with potential hybrid work arrangements. High-value specifics include focus on oncology indications, late-stage clinical development, and cross-disciplinary collaboration within a global pharmaceutical setting.