Scientific Affairs Fellow

Your responsibilities will include: Develop and maintain clinical and technical expertise with key AFS products and therapies inclusive of understanding the clinical practice landscape (medical society guidelines, scientific publications, key clinical trials) to support appropriate evidence considerations. Provide KOLs with content development support for scientific and educational forums supporting BSC technologies. Collaborate with internal cross-functional partners to select symposium venues, program scope, and faculty with strategic scientific content highlighting clinical state of the art. Develop scientific speaker resource materials that can be leveraged by physician speakers. Establish strong collaborative relations with internal cross-functional partners (clinical, marketing, and R&D) to reinforce and align the clinical and commercial messages through scientific affairs. Build and maintain a clinically strategic understanding of data assets (bench, preclinical, clinical, post-market) in partnership with internal functional partners to generate scientifically and clinically relevant evidence sets. Convey KOL input to influence internal strategy relative to evidence gaps, clinical trial design, competitive device features. Develop and execute BSC's evidence generation strategy through the ISR program in partnership with the ISR Chair/Committee, Clinical, HEMA and the Franchise. Minimum Bachelor's degree required in Life Science area; MD or MS / PhD preferred in a related field Minimum 5 years of medical education/clinical/pre-clinical/product development/marketing/field clinical/engineering experience (cardiovascular, structural heart and/or EP preferred); Proven experience in the medical industry (clinical, scientific communications, medical affairs, medical education, product management, product development, R&D, medical sales, or field clinical engineering) and in an FDA-regulated environment preferred Overnight travel (15-25%) to scientific conferences and other meetings within and outside the United States 5 years' experience in Scientific Affairs Prior experience in EP and/or LAAC medical devices Prior experience in academic research and scientific symposia as a participant or organizer Prior experience leading project teams and managing timelines using project management methodologies