Clinical Careers Page

Clinical Study Administrator (CTA level)

Clinical Careers Page(1 month ago)

HybridFull TimeJunior$61,416 - $82,311 (estimated)Clinical Operations
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About this role

A Clinical Trial Associate (Clinical Study Administrator) at ICON supports clinical research studies by overseeing study documentation, regulatory recordkeeping, and local study administration. The role acts as a local contact for study teams and contributes to maintaining inspection-ready trial records while collaborating with cross-functional and external partners.

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Required Skills

  • Document Management
  • eTMF
  • Veeva
  • Vendor Management
  • Regulatory Submissions
  • Clinical Trials
  • ICH-GCP
  • Communication
  • Organization
  • Time Management

Qualifications

  • BS/BA Degree
Clinical Careers Page

About Clinical Careers Page

iconplc.com

ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.

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