Sanofi
biopharma
PharmacovigilanceScientist
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Pharmacovigilance Scientist at Sanofi. Skills: Pharmacovigilance, Safety Surveillance, Risk Management. Manage proactive signal detection. Manage safety management committee activities”
What You'll Achieve.
speed up drug discovery; speed up drug development; find answers for patients; accelerate progress; safety surveillance; identify safety signals; evaluate safety data; analyze safety data; improve people’s lives; delivering compelling growth; treat and protect millions; make drug development quicker; make drug development more effective
Industry & Context.
problem-solving abilities
What They're Looking For.
Must Have
Experience in drug safety and risk management, understanding of drug development, understanding of regulatory guidelines, Demonstrated ability to evaluate, interpret, and synthesize scientific data, Knowledge of pharmacovigilance practices, Knowledge of US regulatory requirements, Knowledge of EU regulatory requirements, Knowledge of signal management, Knowledge of risk management throughout the product lifecycle, Working knowledge of common data processing software, Working knowledge of database systems, medical coding expertise, Strategic mindset, problem-solving abilities, Ability to present and critically discuss safety data, attention to detail, Fluent English, Fluent French
Nice to Have
AI-powered research, data platforms, digital platforms
What You'll Do.
Manage proactive signal detection
Manage safety management committee activities
Coordinate safety evaluations
Author safety evaluations
Respond to safety inquiries
Drive end-to-end signal management process
Serve as core member of Safety Management Team
Drive Safety Management Team agenda
Produce necessary data/outputs
Prepare slide presentations
Facilitate discussions
Present complete safety analysis
Manage safety related activities
Support benefit-risk assessment
Support safety risk management
Support risk minimization activities
Develop Risk Management Plans
Coordinate outsourced activities
Oversee outsourced activities
How You'll Work.
Team & Collaboration
partner with Global Safety Officer; collaborate with safety team; work with diverse teams
Communication Scope
present and critically discuss safety data
Process & Methodology
prioritize and plan effectively
Full Job Description
**Job Title:** Pharmacovigilance Scientist * **Location:** Gentilly/ Campus Lyon Carteret– France # ** _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 Patient Safety & Pharmacovigilance team as a Pharmacovigilance Scientist (PVS) and you’ll support an international, dynamic, and culturally diverse team dedicated to safety surveillance throughout the product lifecycle of a broad range of products. The PVS is a safety expert who is responsible for performing core pharmacovigilance activities on a product, in partnership with the Global Safety Officer (GSO), to identify safety signals, evaluate, and analyze safety data for both marketed products and products in clinical development. **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. Together, we chase the miracles of science to improve people’s lives. **Key Responsibilities:** * _Manages proactive signal detection and safety management committee activities_ * _Coordinates and authors safety evaluations and responses to safety inquiries from internal or external stakeholders (i.e., Health Authorities) in collaboration with the safety team_ * _Drives end-to-end signal management process for assigned products in collaboration with the GSO, on the One Rare Disease portfolio_ * _Serves as a core member (coordinator) of the Safety Management Team, drives the agenda, produces the necessary data/outputs, prepares slide presentations, facilitates discussions & documents conclusions, and presents complete safety analysis_ * _Partners with the Safety Team to manage oth
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