Medical Director, Study Responsible Physician - Late Development, Prostate

Role: Director of Clinical Research Oncology responsible for leading and executing global oncology clinical studies within a matrix team. Objectives include advancing clinical development programs, ensuring study integrity, and supporting regulatory submissions. Responsibilities encompass overseeing study start-up, protocol development, medical review, data interpretation, investigator interactions, and vendor management; collaborating with cross-functional teams such as GCO, Data Management, Biostatistics, Regulatory, and Quality. Qualifications: MD or equivalent with a minimum of 3 years in urology/oncology clinical research; board certification or eligibility in Uro-Oncology preferred; strong knowledge of cancer research, GxP, and clinical trial regulations. Skills: excellent communication, influencing, and leadership; experience in cross-functional team environments; travel up to 20-30%, including international. High-Value: Oncology, Uro-Oncology, clinical development, late-stage trials, cross-functional collaboration, global study oversight, regulatory support. Work setup: Locations include La Jolla, Los Angeles, Raritan, and Spring House with travel requirements.