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Incyte Sr Manager Medical Information & Content Development 
United States, Pennsylvania 
532990605

21.07.2024

Summary of the Essential Functions of the Job

  • Develops content for US Medical Affairs programs and projects including agendas, medical presentations, ad hoc clinical engagements, and internal scientific meetings and select medical congresses, and supports cross-functional execution.
  • Collaborates with cross-functional partners (e.g., Research & Development, US/Global Medical Affairs, Publications & Scientific Communications), to develop scientific exchange materials for emerging therapeutic areas.
  • Manages medical advisory boards, including assistance with identifying external experts, developing, and approving meeting content, and executing the advisory board meeting.
  • Works cross-functionally to develop medical congress scientific booth content related to research targets, investigational agents, and clinical study recruitment.
  • Develops and maintains expertise in dermatology, and IAI therapeutic areas, including disease states, treatment landscape, 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.
  • Participates in the creation and maintenance of departmental SOPs and other guidance documents necessary to ensure highest levels of quality, compliance, and operational efficiency.
  • Assists with creation of medical information standard response letters, product dossiers, and frequently asked question (FAQ) documents, as needed.

Minimum Requirements

  • Advanced scientific or clinical degree in the life sciences (e.g., Pharm.D., or Ph.D); minimum of 2 years' experience working in a Medical Information/Medical Affairs capacity for a pharmaceutical, medical device, medical communications company, or equivalent experience, is required.
  • Experience creating scientific content, including disease state and product-related slide presentations, is required.
  • Experience in the management and execution of advisory boards is preferred.
  • Knowledge of FDA regulations regarding the dissemination of Medical Information and drug promotion, is required.
  • Excellent oral and written communication skills are required.
  • Excellent project management skills, including the ability to plan, prioritize, and execute multiple projects are required.
  • Experience in IAI, especially dermatology, is strongly preferred.
  • Approximately 15% travel commitments.
  • Able to work on-site a minimum of 4 business days per week.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

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