Signal Management Expert
Listed on 2026-09-13
-
Business
Regulatory Compliance Specialist
About The Job
As Signal Management Expert within our R&D team, you will be part of a cutting‑edge safety group dedicated to optimizing the benefit‑risk of our therapies so we can best serve our patients and consumers. The Signal Management team is an international group of process, method, and technology experts dedicated to supporting Global Safety Officers (GSO) and Pharmacovigilance Scientists (PVS) in monitoring product safety throughout the product lifecycle.
JobTitle
Signal Management Expert
- Location:
Morristown, NJ
We're an R&D‑driven, AI‑powered biopharma company committed to improving peoples 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 peoples lives.
Main Responsibilities- Collaborates with stakeholders across PSPV to ensure a compliant and efficient signal management process accounting for interdependencies with other PV and cross functional activities
- Manages the process and systems for routine signal detection and tracking of signal assessment
- Monitors external environment (i.e., regulations, literature, professional societies) for insights and innovation of the Sanofi signal management system
- Partners with Sanofi digital to administer, improve and implement digital systems used to perform signal detection and management
- Understands and evaluates signal detection data sources, methods, and tools to enhance Sanofis safety surveillance processes and systems
- Provides training and ongoing support to roles executing signal detection and signal management processes such as GSOs, PVS, Therapeutic Area Heads, Country Safety Heads
- Coordinates and oversees outsourced PV activities (i.e., maintenance of signal detection schedules, business administration of systems)
- Minimum 2 years of experience in a pharmaceutical, biotech, or other regulated environment
- Evaluation, interpretation, and communication of scientific data
- Experience identifying, evaluating, and implementing process improvement initiatives including corrective and preventative actions (CAPAs)
- Working knowledge of pharmacovigilance and drug safety practices including US and EU regulatory requirements
- Team player that communicates and performs effectively in a cross‑functional, collaborative environment
- Self‑motivated, able to prioritize on impact and a Sanofi first perspective
- Ability to influence across stakeholder groups and levels of the organization
- Working knowledge of common data processing software and database systems
- Ability to map, analyze and measure processes
- Strategic thinker with ability to understand and assess impact of interconnected activities, projects, and systems
- Proficiency with MS applications
- Bachelor's degree in a healthcare, life sciences, or STEM discipline (e.g., Biology, Chemistry, Pharmacy, Public Health, or Biomedical Sciences)
- Preferred advanced degree such as Doctor of Pharmacy, Master of Science, PhD
- English (Business proficiency)
- 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 its 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.
- Be part of a pioneering biopharma…
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).