Medical Affairs Manager, Prescription job

The Medical Affairs Manager serves as an internal scientific expert to support the business unit as representative for a specific Therapeutic area or product.This role acts as a medical affairs interface for the dedicated teams(i.e. sales, marketing, and commercial) supporting, coordinating, and implementing projects according to the business units needs and specifications. This position also provides clear and consistent medical and scientific input throughout the late stage development and commercialization phases for all related products/services in the area of expertise. Collaborates with key internal U.S. and Global stake holders in the business unit (e.g., Medical Affairs, Development, Regulatory, and Commercial colleagues) to generate and provide scientific insights and recommendations in the execution of strategy and tactics, as appropriate. Produces, coordinates, manages, and presents medical and scientific content for given medical area (e.g., abstracts, posters, publications, medical decks, speaker programs, advisory boards)including Medical and strategic review of all deliverables produced by vendor agencies Directs the development of the strategic publication/communication plan and remains current on new data and developments in a given medical area Identifies, develops, and maintains relationships with scientific influencers(MDs, PAs); collaborates with scientific influencers and advocacy partners (professional and patient organizations) to learn of customer needs, scientific gaps, trends, opportunities for clinical trials, business development, etc . Trains external scientific influencers/speakers on content for medical and promotional events; participates in speaker training programs as medical/scientific expert Develops educational materials in collaboration with Marketing and Commercial Excellence to assist in field sales training as needed Ensures the integrity of the scientific data used in all promotional claims and materials Other duties as assigned Travel & Residency Galderma Laboratories, L.P. USA Headquarters; Fort Worth, TXSeven or more years of related medical affairs experience in the pharmaceutical, biotechnology, medical devices and/or CRO (contract research organization) industry Ability to interface effectively with a variety of technical platforms for the collection, review, and dissemination of medical information Solid understanding of FDA, OIG, HIPAA, and other regulatory guidelines relevant to the pharmaceutical industry; related experience within the United States (i.e. understanding of US regulatory environment) Experience within a corporate setting and an understanding of the relationship between marketing/brand teams and medical/regulatory affairs teams is preferred Ability to think strategically to guide publication - related activities in accordance with industry standards and good publication practices Excellent written and verbal communication skills required Proficient with MS Office Meeting planning and facilitation skills required Strong analytical and organization skills required