Medical Affairs Content Developer

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Medical Affairs Content Developer

Contract Term: Anticipated 1 year, potential to renew

Location: Nutley, NJ / Hyrbrid

NOTE: This position will be hybrid, in Nutley, NJ office 2 or 3 times a week.




This role is responsible for the creation and development of scientific and medical content for use by US Medical Affairs and Field Medical external activities and training.

Key responsibilities include:

  • Development of internal and external use materials (i.e. MSL slide decks, advisory board materials, internal training and other scientific exchange resources)
  • Ensure appropriate review and approval processes are followed according to policies and procedures
  • Workflow task management & tracking of multiple projects
  • Ability to collaborate with multiple stakeholders within US and Global Medical Affairs
  • Ensures approved updated versions of documents are accessible to stakeholders
  • May work with external agencies to manage development of content as needed
  • Helps maintain and update reference library



Education and Experience Requirements

  • Advanced degree in medical and/or scientific field preferred (PharmD, PhD, or MS, etc…)
  • 3 years of experience in biopharmaceutical industry preferred
  • Oncology experience required
  • Medical writing experience required
  • Project management experience highly preferred


Key Skills, Competencies and Abilities

  • Strong knowledge and application of Microsoft Office Applications including Excel, PowerPoint, and Word.
  • Veeva experience is preferred.
  • Strong ability to self-manage multiple projects, consistently meet and manage timelines, in addition to organization skills and keen attention to detail and accuracy.
  • Strong written, verbal, and interpersonal communication skills.

• Desire to innovate and work in a fast paced, energetic environment with multiple priorities