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.
Responsibilities:
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:
Advanced degree in medical and/or scientific field preferred (PharmD, PhD, or MS, etc...)
3 years of experience in biopharmaceutical industry
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.