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Specialist II, Quality Control
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- Coordinate and conduct the quality review of source documents to identify protocol deviations, ALCOC and GCP/ICH compliance and logic checks.
- Identify compliance and deviation trends across coordinators and/or trials and escalate to Site Leadership, Investigator and Manager of QC.
- Works closely with QC manager to communicate with Site Leadership and Velocity QA regarding any protocol deviations, good documentation practices deficiencies and any identified potential staff training requirements.
- Participate in site director quality calls to discuss QC findings.
- Bachelor’s degree and minimum of 2 years’ experience as a Clinical Research Coordinator/Clinical Research Associate OR
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