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Regeneron
Regeneron
H1B Visa SponsorBiotechnologyHealthcareManufacturing
Regeneron is a biotechnology company that discovers, develops, and commercializes medicines for serious and underserved conditions. Its research spans allergy, cardiovascular and metabolic disease, neuroscience, oncology, hematology, ophthalmology, and rare diseases. By combining biological research with advanced technology, Regeneron works on biologics and genetic medicines designed to address complex healthcare needs. The company also highlights health equity, environmental responsibility, scientific education, and ethical corporate practices as part of its broader mission to advance patient care.
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Clinical Study Specialist – Regeneron (Hybrid)

Support Regeneron clinical trials by coordinating study operations, site activities, reporting, and close-out across Armonk and Warren.

USUnited StatesNJNew JerseyNYNew York
$93,900 – $153,300 / year
HybridFull-timeJuniorMiddleEnglish RequiredClinical SpecialistGeneral
Google Cloud Platform

Description

  • Provide technical and administrative support to clinical study teams across assigned trial programs
  • Help keep studies on schedule from site activation through close-out
  • Prepare and distribute analyzable reports and performance metrics
  • Plan study team meetings and manage agendas and minutes
  • Compile data for feasibility reviews and site-selection evaluations
  • Assist with reviewing study documents and reference materials
  • Monitor site activation, enrollment, and monitoring visits against forecasted timelines
  • Escalate issues and delays while tracking investigator and site status and registry postings
  • Obtain scheduled reports on time and reconcile TMF records under study lead guidance
  • Communicate with clinical sites and maintain contact details and internal and external relationships
  • Support study close-out activities and help oversee third-party vendors
  • Assess how newly available information may affect ongoing trials
  • Take part in SOP updates and departmental projects
  • Identify and recommend improvements to study processes

Requirements

  • Bachelor’s degree and at least two years of relevant industry experience in a clinical environment
  • Ability to develop working proficiency with trial management systems and Microsoft applications, including Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC, and TMF
  • Basic understanding of medical terminology and clinical drug development
  • Familiarity with ICH/GCP principles
  • Proactive, self-directed, and capable of managing competing deadlines and priorities

Benefits

  • Eligibility for annual bonuses or other incentive programs
  • Potential equity awards
  • Pension or retirement benefits
  • Company-matched 401(k) plan
  • Health and wellness initiatives
  • On-site fitness centers
  • Medical, dental, vision, life, and disability insurance
  • Paid time off
  • Family support programs
  • Reasonable recruitment-process accommodations when required

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