Clinical Research Associate - CRA (All levels)
Core
Conduct remote or on-site clinical monitoring and site management to ensure protocol and regulatory compliance, manage documentation, and guarantee subject rights and data reliability.
Role type
Junior Clinical Research Associate (CRA)
Builds
Clinical trials for pharmaceutical and biotech sponsors
Domain
Life Sciences / Clinical Research
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, data verification (SDR/SDV/CRF), regulatory compliance (ICH-GCP), site initiation, trial close-out, document management
Preferred skills
Medical terminology, anatomy knowledge, clinical trial management systems
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches; ensure data accuracy through document review; initiate and close out clinical trial sites; maintain audit readiness; track trial status and progress; facilitate communication between sites, clients, and internal teams.
Seniority
Junior, hands-on IC