Med. Info. Content Dev. Manager/Sr. Manager

Role Summary

The Medical Information and Content Development Manager/Sr. Mgr. is responsible for providing accurate, timely, unbiased, and up-to-date medical information to internal and external customers. The position involves creating and maintaining written scientific content, including MIRLs, FAQs, and product dossiers for marketed products, investigational compounds, and related disease states. The role also serves as the primary medical reviewer of promotional and sales training materials, and develops US Medical Affairs scientific exchange materials for field staff, advisory boards, medical congresses, and other projects. Reports to the Executive Director, Medical Information and Content Development.

Responsibilities

• Oversee, develop, and maintain written scientific information for responding to unsolicited customer requests; explore opportunities to leverage AI solutions.
• Manage external vendors involved in scientific content development.
• Create medical information standard response letters, product dossiers, and FAQ documents.
• Serve as an active member on cross-functional teams (e.g., promotional materials review committee, core medical team, scientific materials review committee).
• Provide medical literature surveillance for Medical Affairs; communicate pertinent updates in a timely manner.
• Support medical conference activities, including execution of pre- and post-conference deliverables, insights generation, and staffing of medical/scientific booth.
• Collaborate with cross-functional partners; assist with development of scientific exchange materials for emerging therapeutic areas.
• Develop and maintain expertise in hematology and oncology therapeutic areas, including disease states, treatment landscape, and ongoing research strategies.
• Assist Medical Information Leadership with key projects, as needed.
• Comply with all guidelines, policies, legal, regulatory, and compliance requirements.

Qualifications

• Healthcare Professional (PharmD, MD, RPh, PhD in related field) with 2‚Äì5 years' experience in Medical Information/Medical Affairs for a pharmaceutical or medical device company, or equivalent clinical experience.
• Knowledge of FDA regulations regarding dissemination of medical information, drug promotion, and adverse event/product quality complaint reporting.
• Experience creating scientific content, including MIRLs and clinical slide presentations.
• Ability to query scientific literature (PubMed, Embase, Scopus, etc.) and summarize pertinent findings.
• Excellent oral and written communication skills.
• Excellent project management skills with ability to plan, prioritize, and execute multiple projects.
• Experience in hematology/oncology strongly preferred.
• Approximately 15% travel commitments.