Medical Director, Pulmonary

Medical Director, Pulmonary Location: Cambridge, MA / Morristown, NJ About the Job Join the Sanofi team transforming care for patients with immune challenges, rare diseases, cancers, and neurological conditions. As a key member of the Immunology Medical Affairs function, you will act as a product expert and develop integrated medical and scientific strategies for Pulmonary products across the U.S. Your work will partner with clinical, commercial, regulatory, and market‑access teams to generate evidence, support decision‑making, and maximize patient benefits. Main Responsibilities Develop strategy and tactics for a comprehensive Medical Plan (Medical Education, Medical Communications & Publications, Health Outcomes, Safety, and Clinical Research including PhaseIIIB‑IV and Investigator‑Sponsored Trials) and associated annual budget for Pulmonary products. Execute the integrated Medical Plan to ensure on‑time and on‑budget delivery of all tactical activities. Communicate the Medical Plan details and progress to Management, the Core Team, and other execution stakeholders. Provide data evidence to align strategy with clinical development and commercial objectives. Support communication of scientific and medical insights to internal stakeholders and develop strategic Medical Engagement Plans. Provide medical strategy and expertise to Clinical, Commercial, Market‑Access, and Regulatory partners. Ensure cross‑functional alignment to achieve the medical mission of safe and appropriate product use. Lead medical review and approval of promotional and medical materials, ensuring compliance with corporate standards and regulatory regulations. Review and approve regulatory, safety, scientific, and commercially related content. Support the execution of PhaseIIIB‑IV clinical study programs, including protocol development, data analysis and reporting. Oversee conduct of all clinical studies in line with company standards and GCP/ICH regulations. Review and approve Investigator‑Sponsored Trial (IST) concepts/protocols per SOPs. Identify research collaboration opportunities and oversee post‑marketing clinical trials and registries. Ensure timely public presentation of data generated by internal or investigator‑sponsored studies. Partner with US Drug Safety on adverse event and safety signal communication. Identify and communicate product alerts to the Core Team. Maintain relationships with Key Thought Leaders (physicians and researchers) in the therapeutic area. Lead advisory board discussions and support external advisory board activities. Conduct disease‑state and product training for internal and external stakeholders. Stay informed of current developments via literature review, meetings, and professional associations. Perform additional duties as assigned. About You Advance degree in life sciences or pharmaceutical sciences (Ph.D., Pharm.D., PA, NP, or MD with relevant experience). Minimum 5years of experience in Medical Affairs, preferably with Pulmonary or Immunology focus. Proven record of developing and executing medical strategies for U.S. launch and life‑cycle management. Strong knowledge of U.S. healthcare systems, regulatory and payer environment, and public‑health trends. Excellent scientific and clinical judgment and familiarity with clinical trial design and execution. Ability to translate innovative strategies into actionable plans and influence decisions without direct authority. Strong cross‑functional teamwork skills and political acumen. Exceptional communication skills, both written and oral, with superior presentation abilities. Integrity, ethical standards and commitment to high‑quality scientific data. Digital literacy and ability to travel up to 35% of the time for external meetings, trainings, and customer visits. Salary $178,500.00 – $257,833.33 annually; compensation commensurate with experience. Employees may be eligible for company benefit programs. EEO Statement Sanofi Inc. and its U.S. affiliates are Equal Opportunity and affirmative‑action employers. All qualified applicants will receive consideration for employment without regard to protected characteristics. #J-18808-Ljbffr