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 trials for pharmaceutical sponsors
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
Clinical trial monitoring, site management, protocol compliance, data review, ICH-GCP guidelines knowledge, regulatory knowledge
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
Senior, hands-on IC
