Pharmacovigilance Associate - VIE Contract
We couldn't confirm this posting on Sanofi R&D Vaccins's site in our latest checks -- see current similar openings below.
About this opportunity
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.
#LI-EUR
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 !
Job details
How this role compares
Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.
We currently track 39 comparable Associate Pharmacovigilance roles across 22 biopharma companies.
Salary context
2 of 39 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 39 comparable roles
+ 13 more countries
Seniority mix
39 of 39 peers have a known seniority level
Therapeutic area mix
2 of 39 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Currently open similar roles
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.