Duties Responsible for ensuring content quality of Therapeutic Area Medical Review (TAMRC) pieces including having appropriate permissions, fair balance, citations/references, and copyright relating to 5 Therapeutic area(s).
Acts as a Content/editorial reviewer of applicable scientific resources, MSL training, scientific objectives and Medical Information Booth materials to improve the quality speed and efficiency of the TAMRC Review Process. Responsible for the TAMRC Review Process of Medical Booth Materials for 5 TAs medical congress booth materials.
Manage content from submission through final release and production of approved TAMRC pieces from a content/editorial perspective.
Bachelor’s Degree in Journalism or English or equivalent experience required.
4-7 years experience in a Pharmaceutical Medical Affairs, Marketing, Sales or Agency organization, with a solid understanding of the Medical, Legal, and Regulatory review of non-promotional scientific materials and promotional materials required.
Knowledge and familiarity with Medical Affairs, Field Based Medicine and the Medical Science Liaison role.
Demonstrated relationship management and influencing abilities required.
Demonstrated leadership abilities and ability in conflict management, negotiation.
Awareness of FDA regulations.
Demonstrated ability to manage large projects, multi-task and achieved desired results.
Aprimo software experience required.