A leading pharmaceutical company in Cambridge is seeking a Director of Clinical Regulatory Writing to oversee the communication strategy for drug submissions. Candidates should possess a Master's degree (PhD preferred) and experience in oncology drug development. This role involves leading submission activities, managing clinical-regulatory documents, and fostering stakeholder engagement. Flexible work arrangements are respected, with in-person work encouraged at least three days a week. Apply by 24 October 2025 to join a dynamic team. #J-18808-Ljbffr