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Job summary
A leading clinical research organization is seeking a Clinical Research Associate in Argentina to ensure data integrity and compliance with ICH GCP. Responsibilities include remote and on-site monitoring of clinical sites, maintaining study documentation, and working closely with site staff. Candidates should have at least 1 year of monitoring experience and a degree in biological science or a related field. This role is crucial to maintain high-quality research standards.
Qualifications
Minimum 1 year as a clinical monitor with experience in virtual and onsite monitoring.
Proficiency in English is required.
Responsibilities
Ensure compliance with ICH GCP and local regulations.
Monitor site activities and address any issues.
Communicate with site staff for problem-solving.
Perform both virtual and on-site visits to ensure protocol adherence.
Skills
Sound problem solving skills
Initiative
Advance presentation skills
Client-focused approach
Interpersonal communication skills
Time management
Ability to work independently
Attention to detail
Strong computer skills
Education
Educated to degree level in biological science, pharmacy, or health-related discipline
Tools
Clinical Trial Management System (CTMS)
Electronic Document Management System (EDMS)
MS Office (Excel, Word)
Job description
A leading clinical research organization is seeking a Clinical Research Associate in Argentina to ensure data integrity and compliance with ICH GCP. Responsibilities include remote and on-site monitoring of clinical sites, maintaining study documentation, and working closely with site staff. Candidates should have at least 1 year of monitoring experience and a degree in biological science or a related field. This role is crucial to maintain high-quality research standards.