Clinical Research Associate (CRA) - Client dedicated (FSP)
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 clients.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial monitoring activities and site management processes
Domain
Life Sciences / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical monitoring, Risk Based Monitoring (RBM), Root Cause Analysis (RCA), ICH-GCP knowledge, Protocol adherence, Site initiation, Trial close-out, Data review (SDR/SDV/CRF), Investigational product inventory
Preferred skills
Medical/therapeutic area knowledge, Arabic fluency, English fluency, Critical thinking, Problem-solving
Technologies
Clinical Trial Management Systems (CTMS), Microsoft Office
Responsibilities
Monitor investigator sites using a risk-based approach to identify and resolve compliance issues; Conduct on-site and remote monitoring activities including data review and inventory checks; Initiate and close out clinical trial sites in collaboration with clients; Ensure audit readiness and maintain essential study documents; Facilitate communication between sites, clients, and project teams; Respond to regulatory audits and inspections.
Seniority
Mid-level, hands-on IC