Sr CRA (Level I)
Core
Senior Clinical Research Associate conducting remote and on-site monitoring of clinical trial sites to ensure protocol and regulatory compliance.
Role type
Senior IC Clinical Research Associate (Level I)
Builds
Clinical trials for pharmaceutical and biotech sponsors
Domain
Life Sciences / Clinical Research
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, critical thinking, ICH-GCP compliance, site initiation, data review (SDR/SDV/CRF), investigator management, audit readiness
Preferred skills
Medical/therapeutic area knowledge, travel adaptability, process improvement
Technologies
Clinical Trial Management Systems (CTMS), Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches; ensure data accuracy through document review; initiate and manage clinical trial sites; conduct on-site file reviews; respond to audits and inspections; track trial status and progress; facilitate communication between sites, clients, and project teams.
Seniority
Senior, hands-on IC