• Co-develop and implement the Medical Affairs strategic and integrated medical plans across their lead asset • Through cross-functional collaboration, identify data gaps and develop and deliver an integrated evidence generation plan • Provide scientific guidance and tactical execution for medical publication planning, medical education, medical information system development, field medical liaisons, medical communication, RWE, and HEOR • Work closely with clinical development and regulatory professionals as well as strategic alliance partners • Develop and maintain professional relationships with Key Opinion Leaders (physicians and researchers) and relevant professional societies to exchange scientific knowledge and to identify current and future collaboration opportunities • Contribute to the conduct of scientific advisory boards and steering committees and partner with new product planning in executing subject matter expert focus groups in concert with Executive Director, Medical Affairs • Execute on MA strategic imperatives and tactical plans to enhance healthcare practitioner education and improve patient outcomes • Support preparation of clinical sections of relevant regulatory filings to Health Authorities and safety reporting in conjunction with the Executive Medical Director, Medical Affairs • Provide medical review of training materials for medical and commercial employees; contribute to scientific affairs by authorizing and/or reviewing abstracts, presentations and manuscripts for medical and scientific accuracy and content • Work across the organization to develop and implement publication strategies across multiple programs • Evaluate health economics landscape in each disease area in association with HEOR and make recommendations to the outcomes research plan that can support reimbursement and commercial activity • Work closely with commercial and clinical development in writing target product profiles in light of potential life cycle management opportunities • Partner with Marketing, Market Access, and Commercial Operations in concert with the Executive Director, Medical Affairs, in developing Senior Management approved brand plans • Develop, refine, and implement Medical Affairs policies and procedures and SOPs • Partner with various functions in developing an IME/CME strategy and implement process for review and approval; provide medical review of applications for independent medical education grants • Foster research relationships with key research centers in the US and OUS • Interact regularly with key medical subject matter experts along with Executive Director, Medical Affairs • Support the Medical Information function to respond to external requests for information regarding compounds in development and approved products consistent with promotional compliance and regulatory requirements • Provide medical review or support the medical affairs review and approval of promotional and medical materials in compliance with corporate standards and government/industry regulations; partner effectively with commercial organization to develop scientifically rigorous promotional material • Maintain up-to-date knowledge and adherence of all applicable guidance, regulation, and law that mandates the nature in which pharmaceutical organizations function. • Other duties as assigned