Pharmacovigilance Associate - VIE Contract

Sanofi Aventis Singapore Pte. Ltd; Singapore; On-site; SGD 45,000 - 65,000; Full time

Job summary

Sanofi Aventis Singapore Pte. Ltd is seeking a Pharmacovigilance Associate on a VIE contract in Singapore.

You will assist with PV responsibilities ensuring regulatory compliance for Sanofi products in Singapore and support the Country Safety Head in intake, processing and reporting of ICSRs in line with local and global safety requirements. Join Sanofi's mission and work within our Patient Safety & Pharmacovigilance team.

Qualifications

• Degree in pharmacy, medicine, science or related discipline.
• Fluent English (written and verbal).
• Knowledge of EU GVP regulations will be an asset.

Responsibilities

• Collect information on adverse events (AEs) for all Sanofi products.
• Assess and evaluate information against reporting criteria and guidelines.
• Collaborate with external vendor to ensure processing of local ICSRs per SOPs.
• Assist Country Safety Head in safety training and documentation.
• Perform root-cause analysis and implement CAPAs when required.
• Review digital and market research for PV compliance.
• Support safety signal management and documentation of SSIs.

Skills

Medical terminology

Communication

Attention to detail

Teamwork

Microsoft Office

Presentation

Education

Degree in pharmacy, medicine, science

Job description

Pharmacovigilance Associate - VIE Contract

• Location: Singapore, Singapore

• Target start date: 01/03/2027

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.

About the job

As Pharmacovigilance Associate VIE within our Patient Safety & Pharmacovigilance team, you’ll assist with pharmacovigilance responsibilities ensuring corporate and regulatory requirements are met for all Sanofi products in Singapore. You will support the Country Safety Head in the intake, processing and reporting of local Individual Case Safety Reports (ICSRs) in full compliance with local and global safety regulations as required by local Health Authorities.

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.

Ready to get started?

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:

• Collect information on adverse events (AEs) for all Sanofi products
• Assess and evaluate information received against minimal reporting criteria, internal and regulatory guidelines.
• In collaboration with external vendor, ensure processing of local individual case safety reports (ICSRs) is completed in accordance with local and corporate policies and standard operating procedures (SOPs).
• Assist the Country Safety Head in providing education and training on safety topics within Sanofi Singapore, including documentation of attendees and topics covered (new employee training, PV awareness training, training of service providers).
• Perform root cause analysis (RCA) and implement appropriate corrective actions/ preventative actions (CAPAs) when required.
• Review of digital and market research projects to ensure compliance with PV requirements.
• Support the Country Safety Head in signal management activities including documentation of Significant Safety Issues (SSIs).

About you

Experience:

• Knowledge of the European Union’s Good Pharmacovigilance Practices (GVP) regulations and pharmacovigilance guidelines will be an asset.

Soft and technical skills:

• Good understanding of medical terminology.
• Excellent verbal and written communication skills.
• Attention to detail.
• Works well independently and as part of a team.
• Microsoft Office skill.
• Presentation skills.

Education:

• Degree in pharmacy, medicine, science or related discipline.

Languages:

• Fluent English (written and verbal).

Why choose us?

• Be part of a pioneering biopharma company where patient insights shape drug development.
• Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.
• Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.
• Help improve the lives of millions of people globally by making drug development quicker and more effective.
• Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs.
• Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.
• Achieve genuine work-life balance in a supportive R&D environment.

iMove is a unique program tailored for European youth interested in challenging themselves with meaningful assignments across the globe. At Sanofi we have a strong ambition to invest in young talents who will drive the success of Sanofi tomorrow.

Sanofi’s Work Abroad Program, iMove, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our iMove Work Abroad Program is a unique opportunity to make a difference through your work.

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!