Clinical Research Associate (CRA) - All Levels
Core
Conducts remote or on-site monitoring of clinical trial investigator sites to ensure protocol and regulatory compliance, manage documentation, and guarantee data reliability and subject well-being.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trials for pharmaceutical and biotech clients
Domain
Life Sciences / Clinical Research
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, protocol compliance, ICH-GCP knowledge, site initiation, data review (SDR/SDV/CRF), investigator payment processing, regulatory document management
Preferred skills
Medical/therapeutic area knowledge, problem-solving, critical thinking, team collaboration
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches; conduct on-site and remote monitoring activities; initiate clinical trial sites; perform trial close out and material retrieval; ensure audit readiness; track trial status and progress; facilitate communication between sites, clients, and internal teams.
Seniority
All Levels (Entry to Senior)