Clinical Research

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborate with investigators and site staff to facilitate smooth study conduct
• Perform data review and resolution of queries to maintain high-quality clinical data
• Contribute to preparation and review of study documentation, including protocols and clinical study reports
• Take responsibility for clinical trial monitoring deliverables and work collaboratively

Clinical Research jobs in Guatemala

Clinical Research Associate