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Scientist (External CRO Management)

Regeneron
October 1, 2026
Full-time
On-site
Tarrytown, NY
Clinical Research and Development
Role: Bioanalytical Outsourcing Scientist overseeing external CRO bioanalysis for regulated drug development programs. Responsibilities: provide scientific and operational oversight of nonclinical and clinical bioanalytical assays across multiple platforms (LBA, LC/MS, PCR), ensure GLP/GCLP compliance, coordinate assay development, validation, and sample analysis, communicate progress, and manage CRO relationships. Requirements: BS/MS with 10+ years industry experience, hands-on expertise in regulated bioanalysis and assay validation, strong documentation and communication skills, ability to manage timelines and external vendors. Preferred: experience with gene therapies, CAR-T, mAbs, ADCs, and CRO management. High-Value: focus on regulated bioanalysis, assay validation, GLP/GCLP compliance, external CRO oversight, and multiple analytical platforms. Work setup: onsite in Tarrytown, NY.