Remote CRA II – Clinical Trial Monitoring Specialist

Parexel; Argentina; Remote; ARS 75,728,000 - 121,164,000; Full time

Job summary

Parexel’s Functional Service Provider is looking for CRAs II, SR CRAs I and II to join our team in Argentina, Brazil or Mexico. 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.

Qualifications

• Minimum 1 year of monitoring experience as a clinical monitor (virtual and onsite).
• Minimum 3 years for Senior CRA role with monitoring experience (virtual and onsite).
• Minimum 5 years for Senior CRA II with monitoring experience (virtual and onsite).
• Educated to degree level in biological sciences, pharmacy or health-related discipline; nursing is acceptable.
• Proficiency in local language preferred; English is required.

Responsibilities

• Monitor trials to ensure data integrity, quality and compliance with ICH GCP and local requirements.
• Collaborate with Site Manager to ensure sites are protocol compliant and inspection ready.
• Support site management, monitoring, enrollment, database release, and close-out activities.

Skills

English language

Education

Biological sciences / Pharmacy degree

Job description

Parexel’s Functional Service Provider is looking for CRAs II, SR CRAs I and II to join our team in Argentina, Brazil or Mexico. 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.