Precision Medicine Clinical Lab Ops Manager

Regeneron Pharmaceuticals, Inc.

Armonk (NY)

On-site

USD 115,000 - 187,000

Full time

14 days+

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Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Manager, Precision Medicine Clinical Laboratory Operations to oversee clinical laboratory project and program management across therapeutic areas, ensuring that study starts and data delivery stay on track and that risks are effectively managed.

This role collaborates with PM, study teams and central/lab partners to support the portfolio. The position is on-site in Warren, NJ or Armonk, NY, four days per week, and requires a Bachelor's degree with 8+

Qualifications

  • Bachelor's degree required; Master's preferred.
  • 8+ years in pharma/biotech or related cross-disciplinary setting.
  • 5+ years with Clinical Trials, focusing on clinical sample collection.
  • Strong knowledge of clinical laboratory operations, biospecimen logistics and trial requirements.

Responsibilities

  • Perform clinical laboratory portfolio management for complex Regeneron clinical trials and review timelines and risks.
  • Manage and communicate risks to ensure study starts and data delivery meet expectations.
  • Maintain knowledge of central and specialty laboratory processes and serve as a trusted collaborator.
  • Track biomarker strategy delivery schedules and identify risks with mitigation plans.
  • Oversee laboratory operations goals, schedules, testing and data generation across the portfolio.
  • Liaise with internal partners to manage program level clinical laboratory management.
  • Communicate with clinical study teams on laboratory program direction.

Skills

Clinical trial management
Biospecimen logistics
Laboratory operations
Risk management
Cross-functional collaboration
Communication skills

Education

Bachelor's degree
Masters degree preferred

Job description

Regeneron Pharmaceuticals, Inc. is seeking a Manager, Precision Medicine Clinical Laboratory Operations to oversee clinical laboratory project and program management across therapeutic areas, ensuring that study starts and data delivery stay on track and that risks are effectively managed.

This role collaborates with PM, study teams and central/lab partners to support the portfolio. The position is on-site in Warren, NJ or Armonk, NY, four days per week, and requires a Bachelor's degree with 8+

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