Job title: Pharmacovigilance Coordinator

• Location: São Paulo

About the Job

Are you ready to make a real difference in patient safety? Join Sanofi's Patient Safety & Pharmacovigilance (PSPV) team as a Pharmacovigilance Coordinator in São Paulo, Brazil, and play a key role in ensuring the safe and appropriate use of our products. You'll support local safety surveillance activities, handle periodic safety reports (i.e. PBRERs), risk management plans (RMPs), manage Health Authority Safety Requests, develop deep knowledge of the safety profile of the assigned products, and serve as a strategic partner for product launches — connecting global risk management strategies with local regulatory and business needs.

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. Together, we chase the miracles of science to improve people’s lives.

Main responsibilities:

• Ensure local pharmacovigilance activities comply with global, regional and local regulations, supporting the safe use of Sanofi products in Brazil.

• Build and maintain strong cross-functional partnerships with Medical, Regulatory, Quality, Patient Support Program, Call Center, Commercial, Launches Excellence, Legal and Brand teams to carry out and monitor local safety activities.

• Act as a strategic safety partner for product launches, connecting global risk management strategies with local business and regulatory needs across pre-launch, launch and post-launch stages.

• Serve as Local Safety Officer for assigned products, overseeing safety surveillance, signal detection and management, periodic safety reports, and risk management plans.

• Support the development and implementation of Risk Minimization Measures and contribute to local labeling updates and safety documents review.

• Support the Country Safety Head to maintain the local pharmacovigilance quality system, compliance metrics, root cause analyses, corrective actions and inspection readiness activities.

Individual contributors:

• Maintain knowledge of and comply with the principles of Ethics and Integrity, Sanofi policies and codes of conduct that regulate the pharmaceutical market.

• Comply with and promote Sanofi Health, Safety and Environment (HSE) policies, with the aim of preventing accidents, avoiding health risks, promoting employee well-being and reducing environmental impacts resulting from the execution of work activities.

• Support Sanofi Diversity & Inclusion strategy and initiatives to ensure all employees and partners are treated with respect and receive equal opportunities.

About You

• Background in pharmacovigilance, regulatory affairs, quality, medical or clinical development, with experience in safety-related product management.

• Solid knowledge of pharmacovigilance systems and regulations, with the ability to interpret clinical and safety data.

• Experience with safety documents such as Risk Management Plans (RMPs) and Periodic Benefit-Risk Evaluation Reports (PBRERs).

• Appropriate experience with Regulatory Agency interactions.

• Strong interpersonal and communication skills, with the ability to collaborate across international, cross-functional teams.

• Problem-solving mindset with a sense of urgency and the ability to work effectively under pressure.

• Degree in Medicine, Pharmacy, Health Sciences or related field (PhD, MPH or Master's also considered).

• Advanced Professional English is required.

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.

• 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.

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

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

Pursue Progress. Discover Extraordinary.
Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s 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, or gender identity.

#LI-Hybrid

#LI-LAT

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

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!