Clinical Research Associate II
Core
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials to ensure protocol compliance, data integrity, and patient safety.
Role type
Clinical Research Associate (monitoring)
Builds
Clinical trials for pharmaceutical/medical treatments
Domain
Healthcare / Clinical Research
Required skills
Clinical trial monitoring, protocol compliance, data integrity management, ICH-GCP guidelines knowledge, site qualification, query resolution
Preferred skills
Independent work, collaboration, fast-paced environment adaptability
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; Perform data review and resolve queries; Prepare and review study documentation
Seniority
Mid-level (2+ years experience)
