Admin Assistant For Clinical Trials - Exclusive For People With Disabilities

IQVIA Inc

Sao Paulo, SP, Brazil
Hybrid
Maintain trial master file accuracy
Update clinical documents and systems
Handle clinical documentation filing
This role is part of a talent pool exclusively for people with disabilities to assist Clinical Research Associates and Regulatory teams

Job Summary

  • This role is part of a talent pool exclusively for people with disabilities to assist Clinical Research Associates and Regulatory teams.
  • The incumbent will ensure complete and accurate delivery of the Trial Master File by updating and maintaining clinical documents.
  • Candidates must submit their CV and laudo (medical report) as part of the application process.

Matching Summary

This role is part of a talent pool exclusively for people with disabilities to assist Clinical Research Associates and Regulatory teams.

Skills & Requirements

Must-have

  • Maintain Trial Master File accuracy
  • Update clinical documents and systems
  • Handle clinical documentation filing
  • Track Case Report Forms and queries

Nice-to-have

  • Experience in healthcare environment
  • Upper-intermediate English proficiency
  • Excel knowledge appreciated

Key Requirements

  • Bachelor's Degree in Life Sciences (ideal)
  • 1 year experience in healthcare or equivalent
  • Submission of laudo required
  • Hybrid work model in Sao Paulo

Work Rights

Not specified

Tailored Resume

Cover Letter