Associate Manager, Clinical Laboratory Study Management

Regeneron

. Lead and support Clinical Laboratory Study Managers and external functional service provider resources across assigned therapeutic programs and studies .

Posted 10/6/2026full-timeRemote • United StatesJuniorMid-Level💰 $98,100 - $160,100 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical laboratory operations, biospecimen management, and clinical trial processes, with a strong focus on stakeholder management and operational risk resolution to ensure timely delivery of laboratory services.

Highest-signal resume keywords

Clinical Trial ExperienceClinical Laboratory OperationsBiospecimen LogisticsStakeholder ManagementOperational Risk Resolution

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Sample CollectionLaboratory Data CaptureProtocol ComplianceOperational PlanningLifecycle Activities Management

Soft Skills

Problem SolvingCollaborationLeadershipCommunication

Tools & Technologies

RFP DevelopmentBid EvaluationsData Management Systems

Industry Keywords

PharmaceuticalBiotechnologyClinical ResearchBiospecimen ManagementEmerging Technologies

About the role

Key responsibilities & impact

Lead and support Clinical Laboratory Study Managers and external functional service provider resources across assigned therapeutic programs and studies
Partner with clinical study teams, precision medicine leaders, laboratory vendors, CROs, and internal stakeholders to execute sample collection, testing, and data delivery strategies
Oversee operational planning and lifecycle activities for central and specialty laboratory services, including study start-up, execution, and close-out
Monitor clinical sample acquisition and handling activities, ensuring compliance with informed consent requirements and protocol-defined procedures
Provide subject matter expertise on laboratory operations, biospecimen management, and sample-related clinical trial processes
Support vendor selection activities through RFP development, bid evaluations, and scope of work assessments
Collaborate with data management and sample logistics teams to establish processes for laboratory data capture, transfer, blinding, and reporting
Identify operational risks, resolve sample-related issues, and help ensure critical study milestones and laboratory deliverables are achieved on schedule

Requirements

What you’ll need

Bachelor's degree required
Minimum 6-8 years of pharmaceutical, biotechnology, academic, or governmental cross-functional experience required
Minimum 5 years of clinical trial experience with a focus on clinical sample collection
Extensive experience in clinical laboratory operations, biospecimen logistics, and/or clinical study management
Strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery
Demonstrated knowledge of clinical research, scientific principles, and emerging technologies supporting clinical studies
Proven ability to manage stakeholders, lead internal and external meetings, and develop practical solutions to complex operational challenges

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