Admin Assistant For Clinical Trials - Exclusive For People With Disabilities

IQVIA

São Paulo, Brazil
Hybrid
Trial master file delivery
Clinical document management
Tracking clinical data flow
Perform daily administrative activities in conjunction with Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery

Job Summary

  • Perform daily administrative activities in conjunction with Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.
  • Assist with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

Matching Summary

Perform daily administrative activities in conjunction with Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.

Skills & Requirements

Must-have

  • Trial Master File delivery
  • clinical document management
  • tracking clinical data flow
  • project communications
  • Excel knowledge appreciated

Nice-to-have

  • Life sciences background
  • healthcare environment experience
  • strong organizational skills
  • attention to detail

Key Requirements

  • Bachelor's Degree Life sciences ideally
  • 1 years’ experience healthcare environment
  • Upper-intermediate English level
  • Disability status required

Work Rights

Not specified

Tailored Resume

Cover Letter