Clinical Trial Assistant, HYBRID in Wilmington, DE

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