Clinical Research Associate
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
Sr. Clinical Research Associate (CRA II)
Builds
Clinical trial data and documentation for pharmaceutical sponsors
Domain
Clinical research / Pharmaceutical trials
Deliverable
client delivery
Required skills
Clinical trial monitoring, site management, protocol compliance, data integrity, ICH-GCP guidelines, data review, query resolution
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 including protocols and clinical study reports
Seniority
Senior, hands-on IC