Director, Clinical Science - Oncology

Role: Director, Clinical Science - Oncology, leading design, oversight, and interpretation of clinical studies for radiopharmaceuticals across oncology indications. Responsibilities: develop clinical protocols, author key study documents (e.g., CRFs, reports), oversee study execution with cross-functional teams, ensure data quality, support regulatory submissions, and facilitate scientific communication including publications and presentations. Collaborates with investigators, external experts, and stakeholders to advance clinical programs from IND to registration. Requirements: advanced degree (MD, PhD, PharmD), 7-10 years in pharma, with oncology or radiopharmaceutical experience preferred; deep knowledge of GxP, ICH, and clinical development across phases I-III; proven leadership in complex, matrixed environments, with excellent communication skills. HighValue: oncology/radiopharmaceutical focus, clinical development (Phases I-III), regulatory interactions, study protocol development, GxP adherence. WorkSetup: remote within the US, with approximately 25% overnight travel.