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.
Description:
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