US Medical Director Influenza Vaccines

Job title : US Medical Director Influenza Vaccines Location: Morristown, NJ About the job: The North American Medical Team at Sanofi is a high-performing team of Medical leaders who are a trusted source of scientific and medical information and shared insights; effective and innovative strategic partners to our internal and external stakeholders; and dedicated to public health and empowering lives through immunization. We represent diverse experiences and backgrounds which strengthens our team and mirrors the healthcare communities we engage. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. Main Responsibilities: The US Medical Director, Influenza Vaccines will contribute to development and execution of the medical and scientific (non-promotional) strategy for the franchise portfolio in the US. The US Medical Director is accountable for the medical plan within their defined franchise and scope including the medical plan, data generation, scientific exchange, and stakeholder engagement. Strategy (25%) Act as a cross-functional partner to provide support within the US Medical team and work in close partnership with other departments including brand teams and Public Affairs. Play a leadership role in developing, executing, and contributing to the Country Medical Roadmap (CMR) through close collaboration with the Franchise Medical Head as well as demonstrating active involvement in the annual cross-functional brand planning process. Ensure alignment of the US medical strategy with the Global medical strategy through co-creation within the global medical team. Play a leadership role in shaping medical strategy at global, regional, and local levels, ensuring alignment with US Medical strategic objectives, while monitoring publications outlined in the CMP and determining appropriate dissemination to targeted external stakeholders through collaboration with the Franchise Advisor, External Scientific Exchange, and other key personnel, as well as contributing to congresses, publications, and NITAG engagements. Act as the country Medical expert for the Integrated Evidence Generation Plan (iEGP), providing strategic guidance and serving as the key liaison between global Medical, the Principal Investigator (PI), and the US Medical Team on Sanofi-sponsored studies, as delegated by the Franchise Medical Head. External Stakeholder Engagement (25%) Identify, establish, build, grow, and maintain strategic relationships with senior experts, key opinion leaders (KOLs), professional societies, immunization advisory bodies, patient advocacy groups, decision makers and other external stakeholders, acting as SME and fostering scientific engagement to strengthen their understanding of our products and to collaborate on high-priority global studies and scientific initiatives. Provide external scientific education on disease states, epidemiology, and clinical trials of [franchise] product(s), support company positions, and provide guidance on company products and related medical issues. Evaluate Medical educational grant requests stringently in accordance with internal operating procedures and aligned to Country Medical Plan (CMP) Lead external advisory boards organized to support the medical strategic objectives and/or medical plan. Internal Collaboration/Communication (20%) Provide significant scientific expertise within and outside the [franchise] team. Work with cross-functional internal stakeholders, in particular field medical, to development strategic imperatives and downstream strategies and tactics to support our goals. Provide training to field-based medical team on all current and new publications and related assets in collaboration with NA Training Lead. Provide medical guidance to internal Sanofi customers, including contribution of medical information and clinical trial data for pharmacovigilance (PV) and regulatory reports to the US FDA and other health authorities. Collaborate with marketing teams to link sound evidence to brand strategy. Represent as country medical expert in all product label updates and product Company Core Datasheet (CCDS) updates. Data Generation (15%) Work with R&D and Clinical Development teams to provide medical input to the design and support the execution of company-sponsored clinical trials (i.e., Ph 4 post-marketing and observational studies) for new products that may join franchise portfolio in accordance with integrated evidence generation plans (iEGP) Partner with R&D and Clinical Development teams to write, review, edit, and approve key regulatory documents. Engage Key External Leaders (KOLs) to apply for support for ISSs that are aligned with Life Cycle Management and Global Brand Team (GBT) strategies. Liaise with Medical Study Leader to oversee investigator-initiated study (IIS) process from end to end including: Reviewing ISS and ESC applications Liaise with the investigators of study applications. Present studies to the GMT and SRC Follow study progress to completion including eventual publication. Medical Operations (10%) Participate as subject matter expert on multi-disciplinary Review Committee (RC) meetings for medical review and approval of all materials and messaging intended for external use. Contribute to the development and management of specifically owned franchise budget line items by tracking expenditures and executing plans in a cost-effective manner in collaboration with the Franchise Medical Strategy Planner About you Basic Qualifications: Advanced degree (PhD, PharmD, DO, MD) in scientific or healthcare-related discipline (vaccinology, immunology, microbiology, infectious disease, or related field) 5+ years in Medical Affairs within the pharmaceutical / biotechnology industry or related field (public health, academia) Relevant clinical experience or track record of peer reviewed publications in the US Ability to travel up to 20% of the time. Knowledge of US health care system, communicable disease control, public health, and immunization practices Preferred Qualifications: Prior experience in an external stakeholder facing role (i.e., governmental collaboration). Recognized by other vaccine