Job responsibilities To actively contribute to the organization business unit BU TA cluster by taking responsibility for the scientific technical and ethical soundness of all policies statements and endeavors To lead the BU medical team in all activities medically related to the allocated Pfizer Business Unit portfolio and provide high quality and timely service in the areas of medical initiatives support to the assigned portfolio Interactions with Healthcare Professionals Continuing Medical Education Clinical Research Sales Force Training Medical Information and Performance People Management and support in the areas of Recent Product Development Branded Value Offerings Regulatory Affairs Quality Standards and Business Technology A Strategic Policy Provide tactical and strategic inputs and business technical expertise to Product Management towards ethical promotion of assigned products in the operational areas listed B Operational Medical Initiatives support for the Allocated Portfolio New Key Detail In-line Products Provide strategic inputs and support towards creation of marketing brand plans medical development plans and towards design and execution of medical-marketing programs clinical programs including initiatives to enhance access to medicines Initiate and or review and or approve promotional training and Continuing Medical Education CME material in compliance with relevant SOPs regulations industry codes working practices Participate facilitate conduct customized promotional educational interactions with Health Care Professionals HCPs These interactions include but are not limited to customer launch meetings advisory boards CME programs scientific symposia institutional presentations etc C Clinical Research In consultation with concerned stakeholder vendor interface develop write and or review and or approve protocol synopsis final protocols supporting documents per need e g investigators brochure IB informed consent form ICF patient information sheets etc for Phase IV PMS Observational studies surveys Pharmacoeconomic Outcomes Research studies and other clinical projects programs In consultation with concerned stakeholder vendor interface review and approve additional supporting documents databases including ICF CRF SAP etc Assist in planning organizing and preparing Investigational New Drug Applications NDAs Review interpret data generated write final reports for locally sponsored studies as required Develop and execute Publication Plan review approve write manuscripts for publication of locally sponsored studies Develop and execute Information Dissemination Plan Program Medical Information Provide useful timely accurate and balanced medical information to internal sales staff and external HCPs customers in adherence to relevant SOPs policies D Sales Force Training Provide medical training to new sales staff on basic sciences TAs assigned products Provide refresher training to sales staff through ongoing training initiatives Provide pre-launch and launch training to sales staff for new products E New Product Planning Development For global products assist NPP team with preparing business case and pre-commercialization programs initiatives activities to prepare internal and external stakeholders for new product launches These include assistance with market research stakeholder mapping and early access programs Support New Product Planning Marketing and Business Development colleagues with medical evaluation and recommendations on opportunities to launch new products e g licensing acquiring co-promotion etc Support organization efforts at developing local formulations line extensions through literature search recommendations Function as custodian for coordinating internal and regional approvals through the RFD Request For Development process F Regulatory Provide medical and product expertise towards registration of new products indications with federal state regulatory authorities through delivery of scientific presentations provision of medical rationale and published literature and liaison with key HCPs for obtaining support for new product indication Provide medical and product expertise towards defense of marketed products regulators NGOs press etc Write revise and review labeling documents for pipeline local products per relevant SOPs Provide medical support towards processing of spontaneous solicited AE reports per relevant SOPs and or working practices Location On Premise Mumbai Required SkillsDegreein Microbiology preferred MD in Pharmacology Experience in medical affairs Strong scientific and medical knowledge Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates Medical

📌 Medical Advisor (Maharashtra)
🏢 Pfizer
📍 Maharashtra