Senior Biomarker Assay Quality Lead

Regeneron Pharmaceuticals, Inc (USA); United States; Sur place; USD 129 000 - 210 000; Plein temps

Avantages offerts par ce poste

Annual bonus

Equity awards

Pension/retirement benefits

401(k) company match

Health and wellness programs

Paid time off

Résumé du poste

Regeneron Pharmaceuticals, Inc. seeks a Senior Principal Scientist to lead Biomarker Assay Quality within Translational Medicine.

You will oversee assay development, validation, and quality monitoring across multiple platforms, coordinating with internal teams and external labs to ensure robust data for clinical endpoints. The role emphasizes scientific rigor, fit-for-purpose validation, and preanalytical variable control, with an on-site work model (4 days onsite) in Tarrytown, NY.

Qualifications

• Ph.D., M.D., or comparable advanced degree required.
• Proven track record in clinical assay development, validation and implementation.
• Experience with cross-functional teams in pharma/biotech is essential.

Responsabilités

• Provide independent scientific and quality oversight of biomarker assay development, validation, implementation, and ongoing performance.
• Review and approve assay-development scopes of work, analytical validation plans and quality-monitoring plans.
• Collaborate with internal labs and external laboratories to standardize assay documentation and data quality.
• Lead efforts to improve efficiency and harmonize specimen handling and preanalytical variables.

Connaissances

Biomarker assays

Quality oversight

Cross-functional collaboration

Molecular techniques

Formation

Ph.D./MD or equivalent

Description du poste

Regeneron Pharmaceuticals, Inc. seeks a Senior Principal Scientist to lead Biomarker Assay Quality within Translational Medicine.

You will oversee assay development, validation, and quality monitoring across multiple platforms, coordinating with internal teams and external labs to ensure robust data for clinical endpoints. The role emphasizes scientific rigor, fit-for-purpose validation, and preanalytical variable control, with an on-site work model (4 days onsite) in Tarrytown, NY.