Experienced Clinical Research Associate (CRA II/Sr CRA) - AR, KS, LA, MO, OK, TX - Multiple Therapeutic Areas Available
Core
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical and biotech clinical trials.
Role type
Senior Clinical Research Associate (CRA II)
Builds
Clinical trial data integrity and regulatory compliance for sponsors across multiple therapeutic areas
Domain
Life Sciences / Clinical Research / Pharmaceutical
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, protocol compliance, ICH-GCP guidelines, site management, data review (SDR/SDV/CRF), investigational product inventory, audit readiness
Preferred skills
Medical/therapeutic area knowledge, clinical trial management systems (CTMS), process improvement
Technologies
Clinical Trial Management Systems (CTMS), Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches; ensure data accuracy through document and source data verification; manage site initiation and close-out procedures; prepare audit responses and inspection readiness; track trial status and progress reports; facilitate communication between sites, clients, and project teams.
Seniority
Senior, hands-on IC