Key Responsibilities:

• Respond to medical inquiries from healthcare professionals, patients, field staff, and internal stakeholders using clinical and scientific expertise.
• Monitor scientific literature for potential adverse event reports and report findings to Product Safety within designated timelines.
• Conduct in-depth research and analysis of scientific literature on company products, investigational compounds, competitor products, and disease states.
• Contribute to the creation and revision of standard medical response documents, AMCP dossiers, Q&A materials, and other resources.
• Ensure medical accuracy in advertising, promotional, and scientific materials as a member of the Copy Review and Medical Review Committees.
• Ensure scientific information aligns with product labeling.
• Support other Medical Communications and Medical Affairs activities as needed.

Required Knowledge and Skills:

• Advanced degree in biosciences (PharmD preferred).
• Oncology experience is an advantage.
• In-depth knowledge of U.S. regulatory standards for pharmaceutical communications and dissemination of medical information.
• Strong verbal and written communication skills with demonstrated experience in medical writing.
• Expertise in literature database search methodologies.
• Minimum of 1-3 years of experience in medical information within the pharmaceutical industry or a related field.