Lead and execute the Medical strategy for the product portfolio in various stages of clinical development and lifecycle management of products in the assigned therapeutic area. Provide critical input into the strategy, development, management, and implementation of post market clinical or in-vitro studies for the assigned therapeutic area; will also be involved in providing strategic input for global development programs and registration studies. The position includes extensive involvement with global development colleagues, regional marketing, and sales, regulatory, legal and compliance. Publish, present, and communicate scientific information and study data with other disease state experts to help meet the needs of patients and health care practitioners for the assigned therapeutic area.
Drive the execution of comprehensive Medical Affairs strategic plan, including:
- Post Marketing/Phase IV studies/preregistration studies
- Input into launch strategies, life-cycle management, and expansion of indications for use
- Medical Publications: Provide content and strategic direction for whitepapers, peer-reviewed manuscripts, posters, scientific articles, scientific/medical slide deck...
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