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