Medical Affairs Content Developer

Duration: 12+ Months

This position will be hybrid, so the candidate will be expected to work from the 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

Hybrid position is based in Nutley, NJ

Shift: 1st shift