Manager, Clinical Lab Project Management

Regeneron

. Perform clinical laboratory portfolio management for complex Regeneron clinical trials .

Posted 10/6/2026full-timeUnited StatesSeniorLead💰 $114,800 - $187,400 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in clinical laboratory operations and clinical trials management, with a strong focus on biospecimen logistics and risk management. Proficient in liaising with cross-functional teams to ensure alignment on clinical study goals and deliverables.

Highest-signal resume keywords

Clinical Laboratory OperationsClinical Trials ManagementBiospecimen LogisticsRisk ManagementCross-Functional Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Sample CollectionLaboratory Operations DeliveryBiomarker Strategy TrackingMitigation PlanningOperational Decision Implementation

Soft Skills

CommunicationProblem-SolvingTeam Collaboration

Industry Keywords

Pharmaceutical IndustryBiotech IndustryClinical Study KnowledgeCentral Laboratory ProcessesSpecialty Laboratory Processes

About the role

Key responsibilities & impact

Perform clinical laboratory portfolio management for complex Regeneron clinical trials
Review clinical laboratory operations timelines and risks
Manage and communicate risks to ensure study starts and data delivery align with expectations
Leverage central and specialty laboratory process experience to support clinical laboratory deliverables
Track biomarker strategy delivery schedules for clinical development programs and studies
Identify and track risks and decisions and create mitigation plans
Oversee clinical laboratory operations goals, testing schedules, and data generation across the portfolio
Liaise with Precision Medicine Clinical Lab Study Management, Precision Medicine Strategy Leads, Global Development colleagues, and other cross-functional partners
Manage and implement program-level clinical laboratory management
Implement operational decisions for complex non-oncology clinical laboratory trials
Communicate clinical laboratory program direction with clinical study teams and demonstrate study-related program knowledge

Requirements

What you’ll need

Bachelor's degree required
Master's degree preferred
Minimum of 8 years' experience, preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams
Minimum of 5 years' experience with clinical trials, with a focus on clinical sample collection
Extensive experience in clinical laboratory operations, biospecimen logistics, and/or clinical study experience
Strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery
Clinical study knowledge demonstrated by knowledge in science and technology
Active knowledge of central and specialty laboratory processes
Understanding of complex non-oncology clinical laboratory trial requirements
Ability to work remotely within the US or on-site in Warren, NJ or Armonk, NY, with on-site work four days per week if choosing an office location

Benefits

Comp & perks

Annual bonuses or other incentive plans
Equity awards
Pension or retirement benefits
401(k) company match
Health and wellness programs
Fitness centers
Medical, dental, vision, life, and disability insurance benefits
Paid time off
Family support benefits
Reasonable accommodation during the recruitment process where required