Manager, Content Strategy and Development (Medical Writing)- Oncology

Role: Medical Writer (Manager level, Oncology) responsible for preparing clinical/regulatory documents for global submissions, including clinical study reports, protocols, and investigator brochures. Responsibilities: authoring and reviewing documents per regulatory standards, collaborating with cross-functional teams (Regulatory Affairs, Clinical Research, Safety, Data Science), participating in submission strategy, and contributing to document standards and processes. Requirements: 6+ years of relevant experience with BS/BA, 4+ with advanced degrees (MA/MAS/MPH/MBA), or 2+ with PharmD/PhD; proficiency in regulatory document requirements, Microsoft Office, and document management systems. High-Value: oncology, clinical development, regulatory documentation, clinical research environment, experience with global regulatory submissions. Work Setup: not specified; focus on collaboration across multiple teams for global regulatory activities.