Clinical Trial Assistant

IQVIA UK

United Kingdom
Base: $34,400.00 - $118,600.00; bonus/equity: not ...
On-site
Clinical document management
Trial master file (tmf) maintenance
Clinical documentation handling
IQVIA UK is seeking a Clinical Trial Assistant to support clinical research activities by maintaining documentation, assisting with trial supply management, and ensuring compliance with regulatory requirements. The ideal candidate will have a Bachelor’s degree and at least three years of administrative experience, alongside strong communication and organizational skills

Job Summary

  • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems.
  • Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports.
  • Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.

Matching Summary

Match Score: 75

IQVIA UK is seeking a Clinical Trial Assistant to support clinical research activities by maintaining documentation, assisting with trial supply management, and ensuring compliance with regulatory requirements. The ideal candidate will have a Bachelor’s degree and at least three years of administrative experience, alongside strong communication and organizational skills.

Salary

Base: $34,400.00 - $118,600.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Clinical document management
  • Trial Master File (TMF) maintenance
  • Clinical documentation handling
  • Clinical Trial Supplies coordination
  • Clinical data flow tracking

Nice-to-have

  • Site visit assistance
  • Project communication central contact

Key Requirements

  • Bachelor's Degree Required
  • 3 years administrative support experience
  • Computer skills (Word, Excel, PowerPoint)
  • Written and verbal communication skills
  • Effective time management and organizational skills
  • Ability to establish and maintain effective working relationships
  • Awareness of GCP and ICH guidelines
  • Knowledge of applicable protocol requirements

Work Rights

Not specified

Tailored Resume

Cover Letter