Support implementation of US medical affairs strategy for pegcetacoplan in GA in alignment with global medical affairs strategy and cross-functional US initiatives
Assist in implementation of insight gathering, congress planning, KOL engagement plan, and US advisory boards
Collaborate with Field Medical & Global Medical Affairs Strategy to ensure training and resources are available at appropriate times
Serve as a medical reviewer on commercial and medical product review committees
Build and maintain relationships with external stakeholders in the Retina/ophthalmology community
Provide comprehensive training to MSLs and cross-functional partners to enhance their knowledge of data and disease states
Collaborate with cross functional team on approaches to fill identified data and/or communication gaps in alignment with overall strategic objectives
Review sponsorship requests to ensure alignment with areas of focus and budget
Serve as strategic/scientific resource and therapeutic area expert to cross-functional stakeholders
Requirements
5 years+ experience in pharmaceutical/biotechnology medical affairs organization preferred
Experience in Retina/ophthalmology therapeutic area strongly preferred
Agency management experience preferred
Significant experience across drug development stages, particularly in late-stage development, launch, and post approval setting; experience with post-approval research initiatives strongly preferred
Must have a PhD, Pharm D or MD level degree or equivalent