Senior Manager, Precision Medicine Lab Projects

Regeneron Pharmaceuticals, Inc.

Armonk (NY)

On-site

USD 134,000 - 219,000

Full time

14 days+

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Job summary

Regeneron Pharmaceuticals, Inc. seeks a Senior Manager, Precision Medicine Clinical Laboratory Operations to lead portfolio management for clinical laboratory deliverables across therapeutic programs.

You will coordinate with PM, Clinical Trial Management, and Global Development to keep study timelines on track and address risks. The role is on-site in Warren, NJ or Armonk, NY, with four on-site days per week.

Qualifications

  • Bachelor's degree required; master's preferred.
  • 10+ years in pharma/biotech or related cross-disciplinary teams.
  • 5+ years in Clinical Trials with focus on clinical sample collection.
  • Strong understanding of technical, clinical, and strategic aspects of lab operations.

Responsibilities

  • Perform clinical laboratory portfolio management for Regeneron clinical trials and review timelines and risks.
  • Be a subject matter expert on central and specialty laboratory processes and collaborate to ensure deliverables.
  • Keep biomarker strategy delivery schedules on track and create mitigation plans.
  • Manage laboratory operations goals, schedules of testing and data generation.
  • Build strong relationships with cross-functional partners to manage program-level laboratory management.
  • Communicate operational decisions and ensure studies are harmonized from onset to final delivery.
  • Create enhancements to Clinical Laboratory Project Management and address gaps.

Skills

Portfolio management
Cross-functional collaboration
Risk management
Strategic thinking

Education

Bachelor's degree
Master's degree preferred

Job description

Regeneron Pharmaceuticals, Inc. seeks a Senior Manager, Precision Medicine Clinical Laboratory Operations to lead portfolio management for clinical laboratory deliverables across therapeutic programs.

You will coordinate with PM, Clinical Trial Management, and Global Development to keep study timelines on track and address risks. The role is on-site in Warren, NJ or Armonk, NY, with four on-site days per week.

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