Clinical Scientist - Oncology

Role: Clinical Scientist leading regional (US/EU) clinical development of Takeda pipeline compounds. Responsibilities: oversee clinical science activities, contribute to global development strategies, lead protocol development, review safety data, and manage external regulatory interactions. Serve as a key member of multidisciplinary, matrixed teams, influencing development decisions and ensuring alignment with regulatory standards. Requirements: Bachelor's degree with 6+ years (or equivalent advanced degrees with fewer years) in clinical research or development; strong communication, strategic, and negotiation skills; therapeutic area expertise relevant to mechanism of action; knowledge of GCP/ICH and regional regulatory requirements. Preferred skills include experience in planning and executing clinical trials, expertise in GxP, and familiarity with global regulatory processes. High-value specifics: US/EU regulatory engagement, protocol creation, trial oversight, safety assessment, and external stakeholder interaction. Work setup: hybrid in Boston, MA; no travel specified.