Cra II
Core
Conduct clinical trial monitoring activities including site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance, data integrity, and patient safety.
Role type
Clinical Research Associate II (monitoring)
Builds
Clinical trials for pharmaceutical sponsors
Domain
Healthcare / Clinical Research
Required skills
Clinical trial monitoring, site management, protocol compliance, data integrity, ICH-GCP guidelines, query resolution, study documentation
Responsibilities
Conduct site qualification, initiation, monitoring, and close-out visits; Ensure protocol compliance, data integrity, and patient safety; Collaborate with investigators and site staff; Perform data review and resolution of queries; Prepare and review study documentation including protocols and clinical study reports
Seniority
Mid-level, hands-on IC
