
Senior Manager, Aggregate Reporting Management
Regeneron
full-time
Posted on:
Location Type: Remote
Location: United States
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Salary
💰 $134,400 - $219,200 per year
Job Level
Tech Stack
About the role
- Drives preparation, development and maintenance of Aggregate Reporting (i.e., PSURs/PBRER, PAER, DSURs, Local Periodic Reports, SUSARs) Deliverables
- Leads Aggregate Report planning, production and distribution activities across GPS and other functions across US, EU, Japan and other ICH regions, as well as non-ICH regions
- Provides expertise and guidance to authors and contributors of aggregate reports
- Maintains compliance metrics and contributes to implementation of Quality Events and Corrective Action and Preventive Action (CAPA) for non-compliance
- Implements effective structure, procedures and tools to ensure aggregate reports and other functional deliverables are completed timely and with high quality
- Develops and oversees functional specifications of data requirements for aggregate deliverables from the safety and clinical databases
- Collaborates with Global Patient Safety (GPS) and with other functional areas (Epidemiology, Clinical Development, Regulatory Affairs, Statistics, etc.) contributing to aggregate safety reports
- Acts as subject matter expert during audits and inspection.
- Provides oversight, and training as needed of CRO respective activities in support of high quality and timely aggregate reports
- Acts as a functional vendor management overseeing and driving high quality outputs from our vendors
- Develops and maintains aggregate report procedural package (SOPs, Work Instructions), reports’ templates, KPIs
- Drives process improvement through automation and other tech initiatives.
Requirements
- Bachelor’s degree required (advanced degree or HCP‑focused background preferred)
- 5+ years of Pharmacovigilance experience, with a demonstrated focus on Aggregate Safety Reporting.
- Project management experience strongly preferred, PMP preferred
- Experience with health authority inspections (PV and GCP)
- Medical writing experience with regulatory documentation
- Strong project management skills
- Excellent strategic decision-making and analytical skills
- Strong communication and writing skills
- Strong understanding of Scientific content
- Proven experience with technology implementations allowing for streamlined process execution.
Benefits
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Applicant Tracking System Keywords
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Hard Skills & Tools
Aggregate ReportingPSURsPBRERPAERDSURsSUSARsMedical writingProject managementData requirementsProcess improvement
Soft Skills
Strategic decision-makingAnalytical skillsCommunication skillsWriting skillsLeadershipCollaborationTrainingOversightVendor managementExpertise
Certifications
Bachelor's degreePMP