Admin Assistant For Clinical Trials - Exclusive For People With Disabilities

IQVIA UK

São Paulo, SP, Brazil
Hybrid
Trial master file management
Clinical documentation handling
Clinical data flow tracking
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.
  • This is a talent pool for people with disabilities, and if you do not belong to this group and wish to apply, you can apply for other vacancies within IQVIA jobs.

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 management
  • Clinical documentation handling
  • Clinical data flow tracking
  • Project communication central contact

Nice-to-have

  • Life sciences background
  • Healthcare environment experience
  • Excel proficiency

Key Requirements

  • Bachelor's Degree Life sciences ideally
  • 1 year healthcare experience or equivalent
  • Upper-intermediate English level
  • Disability status required for this talent pool

Work Rights

Not specified

Tailored Resume

Cover Letter