Global Periodic Reporting Lead

Job title: Global Periodic Reporting lead
Location: Cambridge, MA / Morristown, NJ / Swiftwater, PA

Join the engine of Sanofis 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.

As Global Periodic Reporting Lead within our Pharmacovigilance team, you will ensure and develop robust, compliant, and controlled processes for Periodic Safety Report (PSR) authoring and vendor oversight. You will lead the Periodic Report Expert (PRE) Team through coaching and mentorship while managing the annual worldwide regulatory planning of PSRs for the entire company portfolio. You will develop and execute outsourcing strategies, uphold regulatory compliance, and drive process improvements to leverage efficiencies.

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

• Ensure and develop robust, compliant, and controlled processes for PSR authoring and vendor oversight while upholding regulatory compliance expectations.
• Lead the Periodic Report Expert (PRE) Team through coaching, mentorship, and development planning according to individual and organizational priorities.
• Develop and execute outsourcing strategies for PSR authoring according to business criticality and resourcing needs.
• Establish and maintain the annual worldwide regulatory planning of PSRs for the entire company portfolio (clinical and postmarketing).
• Manage the PSR Planning Team regarding PSR planning activities, resource allocation, and training needs.
• Serve as system owner for the PSUR Web page Repository and tracking tool database.
• Identify, implement, and support process improvements to leverage efficiencies and drive continuous improvement.

Experience in international pharmacovigilance for marketed drugs and/or projects under clinical development.

Proven track record in transversal collaboration.

Experience compiling and drafting PSRs and safety reports.

• Excellent technical, clinical, and critical analytical skills with keen understanding of clinical safety processes and analysis.
• Strong understanding of global regulatory framework governing PSRs and worldwide pre‑ and postmarketing safety reporting regulations and ICH guidelines.
• Leadership skills including team motivation, problem solving, initiative‑taking, and strong negotiation skills.
• Process improvement experience (LEAN, Continuous Improvement) and project management of multifactorial activities with successful prioritization.
• Excellent written and oral communication skills and computer literacy.

Bachelor’s degree in health science or related field.

Fluent English (written and spoken).

• 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 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.
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high‑quality healthcare, prevention and wellness programs and at least 14 weeks gender‑neutral parental leave.

Sanofi US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, national origin, age, ancestry, nationality, marital, domestic partnership or civil union status, sex, gender, gender identity or expression, affectional or sexual orientation, disability, veteran or military status or liability for military status, domestic violence victim status, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.