Clinical Research Associate
Core
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials while ensuring protocol compliance, data integrity, and patient safety.
Role type
Clinical Research Associate II (IC)
Builds
Clinical trials for pharmaceutical sponsors
Domain
Healthcare / Clinical Research
Required skills
Clinical trial processes, ICH-GCP guidelines, data review, query resolution, site management, regulatory compliance
Preferred skills
None stated
Technologies
None stated
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
Seniority
Mid-level, hands-on IC
