Job Title: Senior Medical Study Leader
Location: Morristown, NJ
About the Job:The Senior Medical Study Leader is a member of the Global Medical Program & Study Management team. He/ She oversees the medical studies from protocol to final study report. He/she contributes to the trial design and manages, coordinates the planning, the feasibility/evaluation and the execution of clinical trials and observational studies performed as part of the Integrated Evidence Generation Plan / Medical Action Plan. The incumbent is responsible for ensuring that the clinical trials and the Observational/Real-World Evidence studies are executed in line with Sanofi strategy in terms of planning, budget, and quality, and according to local and international regulations.
Main Responsibilities:
- The Senior Medical Study Leader is leading/coordinating the clinical trial/study team and works in close collaboration with the Medical Program Leader, Global/Country Medical Expert, Franchise Medical Evidence Generation lead, Pharmaco-Epidemiologist or Epidemiologist, the Clinical Study Management representatives and other functions involved (country release laboratories, external labs, internal labs, Clinical Supply/Commercial Supply Chain, Clinical Study Operations) in the study/trial he/she is responsible of.
- The Senior Medical Study Leader is allocated to a specific Franchise or Product or Region.
- The Senior Medical Study Leader is coordinating and supporting the Medical Study Leader managing studies on their Franchise/Product or the Region they are allocated.
- The Senior Medical Study Leader also contributes significantly to Sanofi initiatives for Process harmonization/improvement/simplification.
About You:Basic Requirements
- Advanced degree (Master's, PhD, MD, PharmD, DVM), or equivalent, in Life Sciences, Biology, Public Health, Clinical Research, Pharmaceutical Sciences, or a related discipline
- Minimum of 8 years of experience in clinical research, project management, or a related field in the pharmaceutical, biopharmaceutical, or biotechnology industry
- Knowledge of GCP/GEP/GPP guidelines and international clinical research regulations
Preferred Qualifications
- Experience in clinical trial management or medical study leadership in vaccines or infectious disease
- Experience overseeing clinical trials and/or real-world evidence studies from protocol to final study report
- Familiarity with Pharmaco-Epidemiology and real-world evidence methodologies
- Experience in international or multi-country clinical studies across more than one regulatory environment
- Professional project management certification (PMP or equivalent)
- Interest in digital tools and their application for real-world evidence generation
Why Choose Us?- Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
- Bring the miracles of science to life alongside a supportive, future-focused team.
- 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.
- Work at the forefront of AI-driven research, smart manufacturing, and groundbreaking mRNA platforms that are redefining the future of immunology.
- Help protect half a billion people every year, contributing to one of the largest global vaccination efforts in healthcare.
- Develop your career with access to mentoring, international mobility programs, and opportunities to grow across four continents.
The salary range for this position is:
$148.500,00 - $214.500,00
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.
