R&D
Where your curiosity drives the
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Job title: Case Medical Strategy Lead

• Location: Morristown, NJ

About the job

Join our Patient Safety and Pharmacovigilance (PSPV) Operations team, as Case Medical Strategy Lead (CMSL) within the Case Management and Medical Evaluation (Vaccines / Specialty Care Unit). 

Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

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 and are supported and enhanced through our diverse portfolio of medical device and diagnostic products. Together, we chase the miracles of science to improve people’s lives.

Main Responsibilities:

• The CMSL provides Case Management expertise, leadership, and mentorship (including product knowledge transfers) of relevant Therapeutic Areas case management members and Service Providers, to ensure appropriate management of cases and related activities.

• The CMSL streamlines, supervises, and ensures consistent case medical oversight activities across GBUs, as developed by GBU Case Medical Safety Lead.

• The CMSL is the focal point for the Case management GBUs on clinical trials and programs safety process expertise, by providing stakeholders with safety process expertise.

• The CMSL is the case medical expert for audits and inspections.

• The CMSL ensures group representation with cross-functional groups within and outside the company (i.e. Therapeutic Areas, Clinical, Quality, Medical, Regional, Business Partners, CRO, Acquisitions and Divestments etc.). 

About you

Education

• MD or Doctor of Pharmacy (PharmD) preferred.

• Other healthcare professionals with adequate patient care experience, or candidates holding a Bachelor's or Master’s degree in Life Sciences or a related field with strong, relevant Pharmacovigilance and case management experience, will also be considered.

Experience

• 8+ years of pharmacovigilance experience, or equivalent relevant pharmaceutical industry experience (clinical development, data management, case management, medical evaluation, etc.).

• Minimum of 3 years of project management/coordination experience is highly desirable.

Soft & Technical skills

• Thorough knowledge of Pharmacovigilance and Medical, Clinical processes and Regulations.

• Expertise of Pharmacovigilance databases and MedDRA coding.

• Ability to influence, demonstrate leadership and establish strong collaborations with cross-functional groups within and outside the company.

• Ability to persuasively communicate ideas and management vision regarding case management strategy in cross functional meetings and working groups.

• Demonstrates initiative and capacity to work under pressure.

• Ability to identify the need for AI use in their assigned activities.

Language

• Fluent in English, able to communicate complex issues, medical and business concepts in English, both verbally and in writing. 

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team.

• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

• Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.

• Help improve the lives of millions of people globally by making drug development quicker and more effective.

• Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Pursue Progress. Discover Extraordinary.

Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.