indeed
CRA/Sr CRA - Client decicated (FSP)
Thermo Fisher Scientific
Riyadh, KSA
Full-time
Onsite
Discovered Today
Clinical monitoringRisk-based monitoringICH-GCPClinical Trial Management SystemRegulatory complianceMedical terminology
Free
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Clinical monitoringRisk-based monitoringICH-GCP
Role Overview
Perform and coordinate clinical monitoring and site management activities for client-sponsored clinical trials.
Ensure trials follow approved protocols, ICH-GCP guidelines, applicable regulations, and standard operating procedures.
Support subject rights, participant well-being, data reliability, audit readiness, and collaborative relationships with investigative sites.
Key Skills for This Role
Clinical monitoringRisk-based monitoringICH-GCPClinical Trial Management SystemRegulatory complianceMedical terminology
Full Job Posting
Work Schedule
- Standard Monday-Friday work schedule.
Environmental Conditions
- Office environment with remote and on-site clinical monitoring visits.
Role Overview
Perform and coordinate clinical monitoring and site management activities for client-sponsored clinical trials.
Ensure trials follow approved protocols, ICH-GCP guidelines, applicable regulations, and standard operating procedures.
Support subject rights, participant well-being, data reliability, audit readiness, and collaborative relationships with investigative sites.
Key Responsibilities
- Monitor investigator sites through risk-based monitoring, source data review, source data verification, and case report form review.
- Investigate site process failures, recommend corrective and preventive actions, document observations, and follow issues through resolution.
- Participate in investigator meetings, identify potential investigators, initiate sites, close out trials, and retrieve trial materials.
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