Clinical Trial Assistant, HYBRID in Wilmington, DE Job at IQVIA, Wilmington, DE

  • IQVIA
  • Wilmington, DE

Job Description

Clinical Trial Assistant position supporting clinical research operations at a contract research organization. Responsibilities include maintaining trial documentation systems, managing clinical supplies and case report forms, and assisting with site monitoring activities in a hybrid arrangement.

Responsibilities

  • Update and maintain clinical documents and Trial Master File systems for compliance tracking
  • Prepare, handle, distribute, and archive clinical documentation following standard procedures
  • Track and manage Case Report Forms, queries, and clinical data flow
  • Assist with handling and distribution of clinical trial supplies and tracking information
  • Serve as central communication contact for project correspondence and documentation

Requirements

  • Bachelor's degree
  • 3 years administrative support experience
  • Proficiency with Microsoft Word, Excel, and PowerPoint
  • Strong written and verbal English communication skills
  • Time management and organizational abilities
  • Knowledge of GCP and ICH guidelines (company-provided training)
  • Understanding of clinical protocol requirements (company-provided training)

Compensation: $35,800.00 - $123,000.00 base

Job Tags

Contract work

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