Manager, Medical Core Content - Rare Diseases

Job Description

The Manager, Medical Core Content is a team-level operational role responsible for the development, maintenance, and day-to-day quality assurance of all core scientific and medical content for the relevant therapeutic area.

This role focuses on the execution and production of scientific assets, ensuring they accurately reflect clinical data, adhere to the core scientific narrative, and are compliant with all internal and external regulations. This position reports directly to the Associate Director, CNS Scientific Communications.

• Under the guidance of the Associate Director, Medical Communications, draft and maintain high-priority, foundational scientific communication core materials, including:

• Core Disease State Decks

• Core Field Materials

• Medical Publications

• New Data Reporting

• Medical Information Content Generation

• Ensure all content adheres to the approved core scientific narrative and lexicon, accurately reflects clinical trial data, and maintains consistency across global materials

• Maintain content repositories and ensure version control and accessibility for global teams

• Utilize platforms like Veeva Vault, to manage content lifecycle and Medical Review submissions.

• Track and report content usage and effectiveness, providing insights for optimization

• Collaborate with Clinical Development and Research teams to integrate new data from clinical study reports or publications into existing core content

• Act as key support resource for the Field Medical Affairs team, managing the content repository and version control for field-facing materials

• Partner with external medical writing agencies, providing operational input and feedback, reviewing drafts for scientific accuracy, and ensuring deliverables align with project timelines

• Ensure all content creation and review processes adhere to internal Standard Operating Procedures (SOPs), Good Publication Practices (GPP), and global regulatory guidelines

• Develop, review, and maintain high-quality, scientifically accurate medical information content for relevant therapeutic area products, including standard response letters, FAQs, and global core content.

• Ensure all content complies with regulatory, legal, and medical standards, and is aligned with product strategy and scientific messaging.

• Collaborate cross-functionally with Medical Affairs, Regulatory, Legal, and Commercial teams to ensure consistency and accuracy of medical communications.

• Support the global-to-local adaptation of core content for use by regional and affiliate medical teams.

• Serve as a champion for Medical Review / Promotional review processes for materials

• Manage content lifecycle processes, including version control, periodic review, and archiving in content management systems (e.g., Veeva Vault).

• Partner with external vendors and internal stakeholders to ensure timely and efficient content development and approval.

• Monitor scientific literature and product data to ensure content reflects the most current evidence and clinical guidance.

• Contribute to the development and implementation of content governance frameworks and best practices.

• Provide training and guidance to internal stakeholders on the appropriate use of medical information content.

• Consider technology and AI to support workflow improvement

• Advanced scientific degree is strongly preferred (Pharm
  
  D, MD, PhD, or equivalent) with expertise in Neuroscience or a related field

• Minimum of 4+ years of applied experience in Medical Affairs, Scientific Communications, Medical Writing, and/or medical information within the pharmaceutical or biotechnology industry

• Proven experience in the development and writing of core medical affairs content (e.g., scientific decks, disease state materials)

• Experience working with medical writing agencies and managing content projects against strict timelines

• Ability to interpret complex scientific data and translate it into clear, concise, and scientifically accurate communication materials for a professional medical audience

• Strong focus on accuracy, consistency, and quality assurance in content creation and version control

• Demonstrated ability to manage multiple content projects and deadlines independently within defined scope and guidance

• Strong verbal and written communication skills to collaborate effectively with internal cross-functional partners and external vendors

• Foundational understanding of the principles governing scientific and medical communications, including GPP and regulatory compliance requirements

Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.

Strategic Thinking & Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the…