CRA（Level II)
Core
Conducts remote or on-site clinical monitoring and site management to ensure protocol compliance, data accuracy, and subject safety across global trials.
Role type
Level II Clinical Research Associate (CRA)
Builds
Clinical trial execution and data integrity for life sciences sponsors
Domain
Clinical Research / Life Sciences
Required skills
Risk-based monitoring, Root cause analysis, Protocol compliance, ICH-GCP knowledge, Site initiation, Data review (SDR/SDV/CRF), Investigational product inventory, Regulatory document management, Clinical trial close-out
Preferred skills
Medical/therapeutic area knowledge, Microsoft Office proficiency, English language skills
Responsibilities
Monitor investigator sites using risk-based approaches; Conduct on-site and remote monitoring visits; Initiate and close out clinical trial sites; Review and ensure completeness of regulatory documents; Track trial status and provide progress reports; Facilitate communication between sites, clients, and project teams; Respond to audits and inspections.
Seniority
Mid-level, hands-on IC