Clinical Trials Assistant 1 (1 Year Contract)

IQVIA

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Trial master file (tmf) maintenance
Clinical document management
Tracking clinical data flow
** IQVIA is seeking a Clinical Trials Assistant for a one-year contract, responsible for supporting Clinical Research Associates and Regulatory teams in the management of clinical documentation and trial master files. The role requires strong administrative skills, attention to detail, and familiarity with clinical research regulations. **

Job Summary

  • Perform daily administrative activities to ensure a complete and accurate Trial Master File delivery.
  • Assist Clinical Research Associates and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems.
  • Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.

Matching Summary

Match Score: 75

** IQVIA is seeking a Clinical Trials Assistant for a one-year contract, responsible for supporting Clinical Research Associates and Regulatory teams in the management of clinical documentation and trial master files. The role requires strong administrative skills, attention to detail, and familiarity with clinical research regulations. **

Skills & Requirements

Must-have

  • Trial Master File (TMF) maintenance
  • Clinical document management
  • Tracking clinical data flow
  • Project communications and correspondence
  • Site compliance tracking

Nice-to-have

  • Effective time management
  • Organizational skills
  • Establish effective working relationships
  • Awareness of GCP and ICH guidelines

Key Requirements

  • High School Diploma or equivalent
  • 3 years administrative support experience
  • Computer skills (Microsoft Word, Excel, PowerPoint)
  • Written and verbal communication skills
  • Applicable clinical research regulatory requirements knowledge

Work Rights

Not specified

Tailored Resume

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