RESPONSIBILITIES:      1.Brand Medical Strategies and Plan and Internal alignment  Involve in all medical affairs activities in the allocated brand/indications/therapeutic area Responsible for representatives of the Therapeutic Area for connection within national Organization, Affiliate cross-functional collaboration 2. Evidence Generation and Communication and Medical Study Lead  Development of local clinical study/Evidence Generation plans. Responsible for identifying and prioritizing the evidence gaps. Conduct of local research activities in a scientific, efficient and compliant way, with due regard to applicable policies, processes and procedures and national regulations, and alignment with areas of strategic research interest for relevant products/therapeutic areas.  3. Medical Compliance Review and Scientific Communications Act as TA representatives on review and approval promotional /non promotional materials and regulatory materials and public affairs materials as needed.  4.EE engagements and External collaboration and Impact ee REQUIREMENTS:                         Medical Degree Strong background in clinical practice Previous medical affairs pharmaceutical or biopharmaceutical industry experience is preferred strong work ethics and compliant behavior Collaborative, team oriented approach, as well as with key external stakeholders. Experience being an active contributor to cross-functional teams and/or working in matrix organizations will be essential.  He/she will possess strong communication and presentation skills. Works broadly across functions to facilitate and support the affiliate’s medical and clinical activities as necessary.