Director of Medical Information and Content Development

1 week ago


Chadds Ford, Pennsylvania, United States Incyte Full time
Job Summary

The Director of Medical Information and Content Development is responsible for identifying needs and developing scientific exchange materials for field-based US Medical Affairs members, ad hoc medical meetings, and other relevant projects and programs. This individual will develop and execute medical advisory boards, including identifying external experts, developing and approving meeting content, and executing the advisory board meeting. The position will also work cross-functionally to plan and develop content for medical congress scientific booths and medical symposia related to disease states of interest, research targets, investigational agents, and clinical study recruitment.

Key Responsibilities
  • Develops content for US Medical Affairs programs and projects, including agendas, medical presentations, ad hoc clinical engagements, select medical congresses, and internal scientific meetings.
  • Manages medical advisory boards, including identifying external experts, developing and approving meeting content, and executing the advisory board meeting.
  • Works cross-functionally to plan and develop content for medical congress scientific booths and medical symposia related to disease states of interest, research targets, investigational agents, and clinical study recruitment.
  • Develops and maintains expertise in dermatology and IAI therapeutic areas, including disease states, treatment modalities, and ongoing research strategies.
  • Provides medical literature surveillance and oversight for US Medical Affairs and identifies and communicates pertinent updates in a timely manner.
  • Manages external vendors, including those involved in scientific content development and advisory boards, and participates in the review and selection process.
  • Collaborates with internal stakeholders to develop and maintain content management solutions.
  • Participates in the creation and maintenance of departmental SOPs necessary to ensure highest levels of quality, compliance, and operational efficiency.
Requirements
  • Advanced scientific or clinical degree in the life sciences (e.g., Pharm.D., or Ph.D).
  • Minimum of 6 years' experience working in a Medical Information/Medical Affairs capacity for a pharmaceutical, medical device, medical communications company, or equivalent experience.
  • Extensive experience creating scientific content, including disease state and product-related slide presentations.
  • Experience in the management and execution of advisory boards.
  • Track record of exhibiting leadership behaviors related to collaborating cross-functionally to build consensus, and executing simultaneous projects in a timely manner.
  • Knowledge of FDA regulations regarding the dissemination of Medical Information and drug promotion.
  • Excellent oral and written communication skills.
  • Excellent project management skills, including the ability to plan, prioritize, and execute multiple projects.


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