Case Medical Strategy Lead

Sanofi•Morristown, NJ

2d•$148,500 - $214,500•Onsite

About The Position

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.

Requirements

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.
8+ years of pharmacovigilance experience, or equivalent relevant pharmaceutical industry experience (clinical development, data management, case management, medical evaluation, etc.).
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.
Fluent in English, able to communicate complex issues, medical and business concepts in English, both verbally and in writing.

Nice To Haves

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

Responsibilities

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.
Streamlines, supervises, and ensures consistent case medical oversight activities across GBUs, as developed by GBU Case Medical Safety Lead.
Is the focal point for the Case management GBUs on clinical trials and programs safety process expertise, by providing stakeholders with safety process expertise.
Is the case medical expert for audits and inspections.
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.).