CRA I/CRA II/Sr CRA
Core
Conduct remote or on-site clinical monitoring visits to assess protocol and regulatory compliance, manage documentation, and ensure data reliability across clinical trials.
Role type
Clinical Research Associate (IC)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical and biotech sponsors
Domain
Life Sciences / Clinical Research
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, data accuracy verification (SDR/SDV/CRF), investigational product inventory, audit readiness, site initiation, trial close-out, ICH-GCP knowledge, medical terminology, Microsoft Office
Preferred skills
Registered Nursing certification, life sciences degree, experience in health sciences with medical training
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches to identify and resolve compliance issues; ensure data accuracy through source data review and CRF checks; manage essential document completion and file reviews; facilitate communication between sites, clients, and internal teams; track trial status and provide progress reports; assist in site identification and initiation; perform trial close-out and material retrieval.
Seniority
Junior to Mid-level, hands-on IC