Clinical Research Associate - 12 months' monitoring experience required
Core
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials to ensure protocol compliance, data integrity, and patient safety.
Role type
Junior Clinical Research Associate (Oncology)
Builds
Clinical trial data and study documentation
Domain
Healthcare / Clinical Research / Oncology
Deliverable
client delivery
Required skills
Clinical trial monitoring, site management, protocol compliance, data integrity, ICH-GCP guidelines, oncology trial experience
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
Junior, hands-on IC
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