Clinical Research Associate (Level II) and above
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
Clinical Research Associate (Level II+)
Builds
Clinical trial execution and site management for top 50 pharma companies and 750+ biotechs
Domain
Life Sciences / Clinical Research / Regulatory Compliance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Risk-based monitoring, root cause analysis, critical thinking, problem-solving, ICH-GCP knowledge, regulatory compliance, data accuracy verification (SDR/SDV/CRF), investigator site management, audit readiness, medical terminology understanding
Preferred skills
Registered Nursing certification, life sciences degree, experience in health sciences with medical training, ability to work independently or in teams
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches to identify failures and implement corrective actions; ensure data accuracy through source data review and CRF checks; assess investigational product inventory and records; initiate and close out clinical trial sites; conduct on-site file reviews; track trial status and provide progress reports; facilitate communication between sites, clients, and internal teams; manage investigator payments and compliance documentation.
Seniority
Mid-level IC (2+ years experience)