CRA 2
Core
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials to ensure protocol compliance, data integrity, and patient safety.
Role type
Mid-level Clinical Research Associate (IC)
Builds
Clinical trial execution and data quality for pharmaceutical/medical device sponsors
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Clinical trial process knowledge, ICH-GCP guidelines, data review, query resolution, site management, travel logistics
Preferred skills
None stated
Technologies
None stated
Responsibilities
Conduct site qualification, initiation, monitoring, and close-out visits; Ensure protocol compliance and data integrity; Collaborate with investigators and site staff; Perform data review and resolve queries; Prepare and review study documentation
Seniority
Mid-level, hands-on IC
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