Clinical Study Specialist

$93.9k - $153.3k

Regeneron Pharmaceuticals, Inc.

Regeneron seeks a Clinical Study Specialist to provide technical and administrative support to clinical trial teams. The role involves managing study timelines, coordinating with sites and stakeholders, tracking enrollment and monitoring activities, and ensuring regulatory compliance across multiple trial programs.

Responsibilities

Generate reports, metrics, and coordinate study team meetings and documentation
Assess feasibility, support site selection, and review clinical trial documents
Track site activation, enrollment, and monitoring visits against project timelines
Ensure timely receipt of regulatory reports and perform TMF reconciliations
Support study close-out activities and maintain site relationships

Requirements

Bachelor's degree with 2+ years of clinical industry work experience
Proficiency in trial management systems, MS Office (Project, PowerPoint, Word, Excel)
Working knowledge of IVRS/IWRS, EDC, and TMF platforms
Basic familiarity with medical terminology and clinical drug development
Awareness of ICH/GCP guidelines
Strong organizational skills and ability to manage competing deadlines

Compensation: $93,900-$153,300 base

Apply

Vacancy posted 2 days ago

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