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Regeneron

Clinical Study Specialist

Regeneron

. Provide technical and administrative support to clinical study teams executing trials across a program .

Posted 9/29/2026full-timeUnited StatesJuniorMid-Level💰 $93,900 - $153,300 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical trial support, including site activation, monitoring, and data management. Proficient in trial management systems and MS applications, with a strong understanding of ICH/GCP guidelines.

Highest-signal resume keywords
Clinical Trial ManagementData ManagementTrial Management SystemsICH/GCP AwarenessMS Applications Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Trial SupportData CollationReport GenerationSite Activation TrackingTMF ReconciliationFeasibility AssessmentStudy Document ReviewEnrollment MonitoringProcess ImprovementSOP Revision
Soft Skills
ProactiveSelf-DisciplinedEffective Time ManagementCommunicationOrganizational Skills
Tools & Technologies
MS ProjectMS PowerPointMS WordMS ExcelIVRS/IWRSEDCTMF
Industry Keywords
Clinical SettingClinical Drug DevelopmentStudy Close-OutThird-Party Vendor OversightSite Monitoring

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Provide technical and administrative support to clinical study teams executing trials across a program
  • Help ensure studies stay on track from site activation through close-out
  • Organize and deliver analyzable reports and metrics
  • Coordinate study team meetings, agendas, and minutes
  • Collate data for feasibility and site selection assessments
  • Contribute to review of study documents and reference materials
  • Track site activation, enrollment, and monitoring visits against projected plans
  • Escalate issues or delays and monitor investigator/site status and registry postings
  • Ensure timely receipt of scheduled reports and perform TMF reconciliations with study lead guidance
  • Communicate with sites and maintain site contact information and internal and external relationships
  • Contribute to close-out activities and support oversight of third-party vendors
  • Investigate the impact of new information on trials
  • Participate in SOP revisions and departmental initiatives
  • Recommend process improvements

Requirements

What you’ll need
  • Bachelor's degree with 2+ years of industry-related work experience in a clinical setting
  • Ability to acquire working knowledge of trial management systems and MS applications (Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC, TMF)
  • Basic familiarity with medical terms and clinical drug development
  • Awareness of ICH/GCP
  • Proactive, self-disciplined, and effective at managing deadlines and priorities

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