We are seeking an experienced CRA based in Argentina to support an exciting early phase CAR-T cell therapy study across the LATAM region.
Contract and Location
1-year contract
Part-time, approximately 10 hours per week
2 active sites in LATAM, with potential for expansion
Key Responsibilities
Conduct remote and on-site monitoring visits across LATAM study sites
Ensure site compliance with protocol, ICH-GCP guidelines, and local regulations
Support site initiation, routine monitoring, and close-out activities
Maintain accurate monitoring visit reports and follow-up documentation
Prepare and submit regulatory packages for site initiation, including ANMAT submissions, ethics committee applications, and supporting documentation in accordance with Argentine regulatory requirements