Freelance Clinical Research Associate

Há 5 dias


Índio do 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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