R&D
Là où votre curiosité fait avancer les miracles de la science

Location: Stockholm, Sweden

Job type: Fixed-term (14 months), Full Time | Hybrid Work Policy

About the Job:

As Pharmacovigilance and Medical Information Officer within our Swedish and North Europe MCO team, you'll be a vital guardian of patient safety—monitoring, reporting, and communicating critical safety information while delivering high-quality medical information guidance to healthcare professionals and patients. Ready to get started?

You'll work at the heart of our commitment to patient safety, handling adverse event reports, managing safety surveillance activities, and responding to medical inquiries. This position combines hands-on Pharmacovigilance and Medical Information activities with active collaboration across the North Europe cluster. Your work directly contributes to the safe and effective use of our medicines in diabetes, transplant, immunology, and other therapeutic areas—helping us deliver on our promise to improve patient outcomes at scale. You'll be at the intersection of regulatory compliance, patient safety, and medical excellence, playing a key role in ensuring that every safety decision upholds Sanofi’s commitment to transforming lives through breakthrough medicines.

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:

• Monitor and report adverse events according to local legislation and company quality standards, ensuring timely and accurate communication to Health Authorities and stakeholders

• Provide expert medical information support to healthcare professionals, patients, and internal teams, delivering high-quality responses to complex medical inquiries

• Support local safety surveillance activities, including risk management, product alerts, and market research programs in collaboration with the Country Safety Head

• Maintain comprehensive knowledge of pharmacovigilance regulations, medical information procedures, and the safety profiles of our product portfolio

• Collaborate with third-party partners and internal teams across the North Europe cluster to ensure seamless PV and MI operations

• Contribute actively to team projects and continuous improvement initiatives within the North Europe Pharmacovigilance and Medical Information team

• Ensure compliance with all regulatory requirements and company quality documents related to patient safety and medical information

About You:

• Experience: Background in the pharmaceutical industry, pharmacy practice, or related healthcare settings, ideally with exposure to pharmacovigilance or medical information activities

• Core Competencies: Strong planning and organizational skills with meticulous attention to detail; ability to work accurately under regulatory and compliance requirements; proven ability to manage multiple priorities effectively

• Communication Skills: Excellent written and verbal communication abilities; comfortable interacting with healthcare professionals, patients, and cross-functional colleagues; strong interpersonal skills with a collaborative mindset

• Technical Skills: Proficient with MS Office and relevant software systems; comfortable learning and working with pharmacovigilance databases and tools

• Languages: Fluent in English and Swedish (written and spoken)

• Education: University degree in Pharmacy, Medicine, or equivalent field

Why Choose Us?

• Protect patient safety by playing a critical role in monitoring and communicating the safety of medicines used by millions

• Make a global impact while working locally across the North Europe region in diabetes, transplant, immunology, and specialty care

• Collaborate across borders with diverse teams of safety experts, medical professionals, and regulatory specialists

• Develop specialized expertise in pharmacovigilance and medical information—highly valued skills in the pharmaceutical industry

• Grow your career in a streamlined, AI-powered organization that values smart, modern ways of working

• Contribute to innovation that improves patient outcomes, relieves pressure on healthcare systems, and expands access worldwide

• Join an inclusive workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice

#LI-EUR

null

Toujours Progresser. Découvrir l’Extraordinaire.

Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.

Chez Sanofi, nous croyons dans l’égalité des chances, sans distinction de race, de couleur, d’ascendance, de religion, de sexe, d’origine, d’orientation sexuelle, d’âge, de citoyenneté, d’état civil, de handicap, d’identité de genre ou de tout autre critère protégé par la loi.