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- FSP Primary

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Argentina, Remote Additional Locations: Brazil, Remote; Mexico, Remote Job ID R0000040020 Category Clinical Trials Apply Now About This Role Parexel’s Functional Service Provider (FSP) is looking for CRAs II, SR CRAs I and II to join our team in Argentina, Brazil, Mexico or Chile. The Clinical Research Associate II 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 II will collaborate with the Site Manager to assure that the site is in compliance with the protocol and is inspection ready. The Senior Clinical Research Associate I (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and client standards. The Sr. CRA is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g. enrollment, database release), to safeguard the quality of investigator sites (e.g. patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance the company’s image with its external stakeholders. The Sr. CRA is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the set-up, running and close-out of sites in a clinical trial. Knowledge And Experience
- For the Clinical Research Associate a mininum of 1 year as a clinical monitor with demonstrated experience of monitoring (virtual & onsite).
- For the Senior Clinical Research Associate a mininum of 3 years as a clinical monitor with demonstrated experience of monitoring (virtual & onsite).
- For the Senior Clinical Research Associate ii a mininum of 5 years as a clinical monitor with demonstrated experience of monitoring (virtual & onsite). Education
- Educated to degree level (biological science, pharmacy, or other health-related discipline preferred)



or equivalent nursing qualification or other equivalent experience
- Proficiency in local language preferred. English is required Apply Now Share this Page
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- CRA II/SR CRA/ SR CRA II
- FSP Argentina, Remote View All Jobs There is no jobs to view You currently have no saved jobs to view. Make sure to accept the Functional cookies to enable this module to display saved job links. You will be able to review them here when you revisit this page.. View Open Positions More Than A Job Benefits Benefits vary by country, but Parexel is passionate about our team’s overall wellness. Learn More Career Advancement We believe that investing in your professional and personal development is an investment in Parexel, and we want to help you realize your full potential and career. Learn More

📌 CRA II/SR CRA/ SR CRA II (Argentina)
🏢 ATLAS MEDICAL SERVICES LTD. STI.
📍 Argentina