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Senior Specialist, Quality Control
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Full-time
- Coordinate and conduct the quality review of source documents to identify protocol deviations, ALCOC and GCP/ICH compliance and logic checks.
- Consistently identify compliance and deviation trends across coordinators and/or trials and escalate to Site Leadership, Investigator and Manager of QC.
- Lead site director quality calls to discuss QC findings.
- Capable of traveling up to 10%, as needed for on-site QC activities and other meetings as required.
- Bachelor’s degree and a minimum of 4 years’ experience as a Clinical Research Coordinator/Clinical Research Associate OR
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