Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l’international, l'anglais étant la langue de travail.
This job offer is accessible to all, regardless of gender.
Job Title: Global Safety Officer
Location: Gentilly
About the job
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. Join our I&I PSPV team as GSO and you’ll be the safety expert for I&I products under development, the top priority of the company, while enjoying lots of opportunities to broaden your experience and hone your skills.
We’re an innovative global healthcare company that helps the world stay ahead of I&I diseases. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
Main responsibilities

Be the Internal & External Safety Expert for I&I products under development
Communicate with and represent PV analyses and PV position within project/product teams, in safety governance and benefit‑risk governance activities and committees (e.g. Safety Management Committee, Benefit‑Risk Assessment Committee), with external partners, key opinion leaders, and Health Authorities, and during internal and external negotiations
Lead Signal Detection & Assessment
Be responsible for Risk Assessment & Risk Management & Benefit‑Risk Assessment
Contribute to Submission Activities

About you
Knowledge & Skills

Excellent clinical judgment
Capability to synthesize and critically analyze data from multiple sources
Ability to communicate complex clinical issues and analysis orally and in writing
Able to develop and document sound risk assessment
Demonstrates initiative and capacity to work under pressure
Demonstrates leadership within cross‑functional team environment
Excellent teamwork and interpersonal skills are required
Fluent in English (written and spoken)

Formal Education & Experience Required

M.D. Degree
For MD, Board Certified/Board eligible, or equivalent, is preferred
For M.D., minimum 3 years’ and for other degrees, minimum 5 years’ total experience in international pharmacovigilance, or equivalent relevant industry experience (e.g. clinical development) with relevant clinical experience considered. Exceptionally, candidates may be considered if they have proven excellence in a similar prior position, even if they have less than 3 years international PV experience

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

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
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Pursue progress, discover extraordinary together.
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