Regeneron
Healthcare
SeniorManagerTriage
Neural analysis suggests this role is
optimal for Manager candidates.
“Senior Manager Triage at Regeneron. Skills: Triage, Pharmacovigilance, Case processing. Lead triage of ICSRs. Oversee team of healthcare professionals”
Industry & Context.
Clinical judgment; Timely decisions; Accurate decisions
What They're Looking For.
Must Have
MD / MBBS, PharmD, BDS, MDS, or Nurse Practitioner, 8+ years total industry experience, 5+ years pharmacovigilance case processing experience, Hands-on ICSR intake experience, Hands-on Argus Safety experience, Hands-on expedited reporting experience, Experience handling high-volume case processing
Nice to Have
Prior experience in triage, Prior first-line safety review experience
What You'll Do.
Oversee team of healthcare professionals
Perform medical triage of ICSRs
Apply expedited reporting logic
Verify source completeness
Identify follow-up requirements
Assign cases to Argus workflow
Escalate complex cases
Author structured summaries for cases
Maintain compliance with SOPs
Maintain data privacy standards
Maintain inspection readiness
Develop innovative approaches to enhance efficiency
Integrate new technologies
How You'll Work.
Team & Collaboration
Downstream pharmacovigilance operations
Communication Scope
Written communication; Case summaries
Full Job Description
**About Regeneron** Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. As a Senior Manager, Triage Team Lead, you will lead the triage of Individual Case Safety Reports (ICSRs) within Argus Safety and oversee a team of healthcare professionals responsible for upfront medical triage activities. This role plays a critical part in ensuring accurate case assessment, regulatory compliance, and inspection-ready documentation while supporting downstream pharmacovigilance operations. **This position is office-based and will be onsite at Regeneron’s India office.** **A Typical Day May Include:** * Performing medical triage of incoming ICSRs within defined timelines, including assessment of seriousness, expectedness, and causality * Applying expedited vs. non-expedited reporting logic, including 7-day and 15-day reporting requirements * Verifying source completeness using standardized intake checklists and identifying follow-up requirements * Assigning cases to the appropriate Argus workflow based on reporting criteria and data completeness * Escalating complex cases to the Lead Medical Reviewer as needed * Authoring structured summaries for serious and high-risk cases, including patient profile, suspect product, adverse events, clinical course, causality assessment, and key review considerations * Maintaining compliance with SOPs, data privacy standards, and inspection readiness requirements * Developing innovative approaches to enhance operational efficiency through integration of new technologies, including AI **This Role May Be for You If You Have:** * Strong knowledge of ICH E2A, E2B, and E2D guidelin
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