Clinical Research Associate
Core
Coordinate clinical monitoring and site management to ensure protocol and regulatory compliance across global trials.
Role type
Clinical Research Associate (monitoring)
Builds
Clinical trial data integrity and regulatory compliance
Domain
Pharmaceutical/Biotech clinical trials
Required skills
Clinical monitoring, ICH-GCP guidelines, risk-based monitoring, root cause analysis, data review (SDR/SDV/CRF), site initiation, audit readiness, travel management
Preferred skills
Life sciences background, nursing certification, therapeutic area knowledge, Microsoft Office
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites for compliance and data accuracy, initiate clinical trial sites, conduct file reviews, track trial status, respond to audits, manage travel and site visits
Seniority
Mid-level, hands-on IC