Associate Manager, Clinical Imaging Operations

Regeneron

. Execute key operational aspects of complex early- and late-phase clinical trials supporting the general medicine portfolio .

Posted 9/29/2026full-timeUnited StatesJuniorMid-Level💰 $109,900 - $179,300 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing complex clinical trial operations with a focus on imaging, ensuring compliance, data integrity, and high-quality image acquisition. Proficient in vendor management, documentation, and providing technical support to clinical site personnel.

Highest-signal resume keywords

Clinical Trial ExperienceImaging Vendor ManagementRegulatory Inspection ExperienceSite Start-Up LogisticsClinical Imaging Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementImaging ProceduresData IntegrityVendor SelectionTimeline ManagementDocumentation ManagementAudit-Ready DocumentationTraining Material ReviewIssue ResolutionPerformance Monitoring

Soft Skills

CollaborationCommunicationProblem-SolvingTechnical SupportTraining

Certifications & Qualifications

BA/BS Degree

Industry Keywords

Clinical ImagingCROsTrial Master FileIndependent Review ChartersSOPsWork InstructionsSite Initiation VisitsCamera QualificationImaging FacilitiesData Transmittal Forms

About the role

Key responsibilities & impact

Execute key operational aspects of complex early- and late-phase clinical trials supporting the general medicine portfolio
Collaborate with Clinical Imaging Science Leads and clinical study teams to ensure high-quality image acquisition, data integrity, and compliance with study-specific imaging procedures
Collaborate with imaging vendors, clinical operations, data management, CROs, and clinical sites throughout study startup, execution, and closeout
Manage imaging startup activities, including vendor selection, requests for proposals, and timeline management
Oversee external imaging vendors at the study level
Author, review, and manage Imaging Manuals, Independent Review Charters, communication plans, data transmittal forms, SOPs, and Work Instructions
Ensure documentation is audit-ready and properly filed in the Trial Master File
Provide technical support and training to clinical site personnel, including site initiation visits or teleconferences
Review and approve training materials for imaging facilities and clinical site personnel
Track imaging progress, resolve issues, monitor imaging performance indicators, support query resolution, and troubleshoot timeliness and quality concerns

Requirements

What you’ll need

Basic knowledge of clinical imaging
Familiarity with imaging vendor processes
BA/BS degree
3+ years of clinical trial experience
Focus on imaging preferred
Experience implementing complex site start-up logistics, such as site training and camera qualification, preferred
Regulatory inspection experience preferred
Ability to work on-site four days per week in Tarrytown, NY, Warren, NJ, or Cambridge, MA

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