Freelance Clinical Research Associate

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!