Parexel FSP is looking for CRAs to join our team in Argentina . We are looking for candidates with +1 year of monitoring experience, based in Buenos Aires.

The Clinical Research Associate will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with the Study Monitoring Plan and will be performed virtually for the majority of activities to supplement on‑site visit requirements. The Clinical Research Associate will collaborate with the Site Manager to assure that the site is in compliance with the protocol and is inspection ready.

Key Accountabilities

Maintenance (from initiation through close out)

• Act as PAREXEL’s direct contact with assigned sites, assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites, and perform problem‑solving to a...