Clinical Trial Assistant- Wilmington, De

IQVIA

Wilmington, Delaware, United States
Base: $34,400.00 - $118,600.00; bonus/equity: ince...
Clinical document management
Trial master file (tmf) maintenance
Clinical documentation handling
Assist Clinical Research Associates and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems

Job Summary

  • Assist Clinical Research Associates and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems.
  • Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports.
  • Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.

Matching Summary

Assist Clinical Research Associates and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems.

Salary

Base: $34,400.00 - $118,600.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits

Skills & Requirements

Must-have

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

Nice-to-have

  • Effective time management
  • Organizational skills
  • Establish working relationships
  • Awareness of regulatory requirements

Key Requirements

  • Bachelor's Degree Required
  • 3 years administrative support experience
  • Equivalent education, training, experience
  • Microsoft Word, Excel, PowerPoint skills
  • Written and verbal communication skills
  • Applicable clinical research regulatory knowledge
  • Applicable protocol requirements knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter