Clinical Research Associate - Fsp

Parexel is looking for multiple **CRAs** with 1+ year of experience in Mexico!
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 address and resolve site issues.
- Build relationships with investigators and site staff.
- Facilitate and support site with acces...