Freelance Clinical Research Associate

1 semana atrás

João Pessoa, Brasil IQVIA Tempo inteiro

Join IQVIA Biotech as a Freelance CRA supporting Phase 2 and 3 clinical trials. You’ll lead site visits, monitor compliance, and ensure high-quality data—all while working with a passionate team.

We currently have two projects in Brazil:
Location: Brazil - travel required for both roles across Brazil
Hours: 1 x 0.35 FTE and 1 x 0.6 FTE
Start: ASAP
Duration: 6 months

Your Role
Conduct site evaluations, initiations, monitoring & close-outs
Ensure GCP compliance and data integrity
Collaborate with investigators and internal teams
Review protocols, study manuals, and eCRFs
Support site staff with training and issue resolution
Track investigational product inventory and documentation
Attend investigator meetings and study-related events
Contribute to audit readiness and inspection support

Your Profile:
2+ years CRA including site monitoring experience
IQVIA monitoring experience
Strong knowledge of clinical trial processes & GCP
Excellent communication & organizational skills
Ability to work independently and manage priorities
Fluent in English and Portuguese

If you're ready to make an impact in clinical research, apply today

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