Pharmacovigilance Associate - VIE Contract

Sanofi; Singapore; On-site; SGD 42,000 - 60,000; Full time

Job summary

Sanofi Singapore is seeking a Pharmacovigilance Associate on a VIE contract to join the Patient Safety & Pharmacovigilance team. You will assist with intake, processing and reporting of local ICSRs in full compliance with local and global safety regulations.

You will collaborate with the Country Safety Head to provide PV education and training, support signal management activities and ensure PV compliance across Sanofi products in Singapore.

Qualifications

• Knowledge of EU Good Pharmacovigilance Practices (GVP) regulations is an asset.
• Strong medical terminology understanding and ability to interpret clinical data.
• Excellent verbal and written communication skills in English.

Responsibilities

• Collect information on adverse events (AEs) for Sanofi products.
• Assess information against reporting criteria and guidelines.
• Ensure ICSR processing aligns with local SOPs and policies.
• Support Country Safety Head with PV training and documentation.

Skills

GVP knowledge

Medical terminology

Communication skills

Attention to detail

Teamwork

Education

Pharmacy degree

Related discipline

Tools

Microsoft Office

Job description

Pharmacovigilance Associate - VIE Contract

Location: Singapore, Singapore

Target start date: 01/03/2027

Program: iMove, the Sanofi VIE Program

Eligibility: Citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28. Applicants must submit applications in English.

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.

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.

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.

We are 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.

Discover more about us visiting www.sanofi.com or via our movie