Clinical Research

• Contribute to the development and execution of clinical strategies for breast cancer programs.
• Maintain a focus on accelerating timelines while ensuring quality.
• Demonstrate compliance with procedures and be accountable for compliance of team members.
• Lead completion of clinical trial documents including protocols, amendments, investigator brochures, informed consent forms, and clinical study reports.
• Supervise and participate in medical monitoring activities, including data review, safety assessments, and protocol deviation management.
• Collaborate with Global Medical Leads, statisticians, and clinical operations to ensure scientific integrity and operational excellence.
• Collaborate with Global Patient Safety on risk management planning.
• Serve as a resource for sites, monitors, investigators, and ethics committees to address study-related questions.
• Provide scientific input for site selection, investigator meetings, steering committees, and clinical trial training.
• Participate in data analysis, scientific dissemination, and preparation of final study reports.
• Analyze and contextualize clinical data to support decision-making and portfolio strategy.
• Contribute to strategic planning and innovation through cross-functional working groups.
• Support planning and execution of symposia, advisory boards, and other external engagements.
• Develop and review scientific materials including slide decks, abstracts, posters, and manuscripts.
• Support regulatory submissions (e.g., INDs, NDAs, BLAs) and prepare materials for health authority interactions.

Clinical Research Scientist – Breast Cancer Franchise

Oncology Early Stage Clinical Scientist – Director, Non-MD

Oncology Early Stage Clinical Scientist – Director, Non-MD

Senior Director, Clinical Scientist – Neuroscience

Late Stage Oncology Clinical Scientist, Director