Joel Davis

Background

About Joel Davis

Major responsibilities included evidence generation, clinical trial design, manuscript development and leading the Medical review for promotional materials. In previous roles, responsibilities included Regulatory Ad Promo review including providing direction and review of promotional materials for the Dermatology team, execution of several CFL promotional campaigns, ensuring adherence to FDA regulations & guidance documents to provide a truthful, non-misleading message to healthcare professionals and patients to support the safe use of AbbVie products, including 3 blockbuster dermatologic biologic and small molecule therapies. Previous roles included the development and execution of strategy and tactics related to Dermatology Pipeline assets to ensure internal launch readiness as well as engaging external experts to inform evidence and education needs. External engagement included the planning and execution of advisory boards, conference based individual consultancies, development of internal advisory councils, and expert mapping. Educational efforts included the design and execution of scientific booths at major dermatology congresses, development of content and execution for symposia. Internal readiness includes the development and execution of face-to-face global disease state training, cross functional education planning and educational content development for broad enterprise implementation. Previous roles also included the review of global promotional materials for medical accuracy and scientific balance, supporting the Global Commercial and Medical Affairs teams by providing launch support for multiple indications of a single asset, providing review of strategic and tactical development, and exhibit booth review for congresses. Role also includes the review of materials utilized for payer interactions by Market Access groups. Experience includes the development and communication of unbiased, scientific, fair balanced medical information to customers, enable healthcare professionals to make healthcare decisions. Additional experience includes an in-house Clinical Research Associate, assisting in coordinating and managing studies from an in-house perspective. Furthermore, experience includes six years in a high acuity intensive care unit specializing in cardiovascular care.