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 operations and data quality
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
International travel experience, driving license
Technologies
Clinical trial management systems (implied by context)
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