Clinical Research Associate II - Adelaide or Perth
Core
Managing and monitoring clinical trials to ensure regulatory compliance, data integrity, and subject protection across investigative sites.
Role type
Senior Clinical Research Associate (On-site Monitoring)
Builds
Clinical trial data and regulatory compliance for healthcare sponsors
Domain
Clinical Research / Healthcare
Deliverable
client delivery
Required skills
ICH GCP guidelines, clinical trial monitoring procedures, source data verification, informed consent verification, adverse event reporting, site management, regulatory document management, travel logistics
Preferred skills
Lead CRA experience, training new employees, matrix environment navigation
Technologies
eClinical systems, trial management tools, eTMF
Responsibilities
Conduct pre-study, initiation, routine, and close-out site monitoring visits; verify source data and resolve queries; ensure informed consent and protocol adherence; track investigational product inventory; prepare monitoring plans and trip reports; assist with investigator recruitment and training.
Seniority
Mid-level, independent execution