Clinical Research Associate - 12 months' monitoring experience required
Core
Conduct clinical trial monitoring activities including site visits, data review, and protocol compliance to ensure patient safety and data integrity for oncology trials.
Role type
Clinical Research Associate (CRA II)
Builds
Clinical trial data and documentation for oncology studies
Domain
Healthcare / Clinical Trials / Oncology
Deliverable
client delivery
Required skills
Clinical trial monitoring, site qualification, protocol compliance, data integrity management, ICH-GCP guidelines knowledge, oncology trial experience
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
