CRA II - Saudi Arabia
Core
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical clinical trials.
Role type
Clinical Research Associate (Level II)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical sponsors
Domain
Life Sciences / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical monitoring, Root cause analysis, Risk-based monitoring, ICH-GCP knowledge, Medical terminology, Arabic fluency, English fluency, Microsoft Office
Preferred skills
Registered Nursing certification, PPD Drug Development Fellowship completion, Site initiation experience
Technologies
Clinical Trial Management System
Responsibilities
Monitor investigator sites using risk-based approaches, conduct on-site file reviews, initiate clinical trial sites, perform trial close out, respond to audits/inspections, provide trial status tracking reports
Seniority
Entry-level to Mid-level, hands-on IC