Senior Clinical Trials Monitor & Auditor
Listed on 2026-10-07
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Business
Regulatory Compliance Specialist
Guidehouse is seeking an experienced Clinical Trial Operations professional to schedule site visits, develop monitoring plans, and review trial documentation across multiple studies. You will identify corrective actions, coordinate with internal and site staff, and ensure timely issue resolution in line with IRB and FDA guidelines.
The role requires a Master’s degree in biology or life sciences and 8+ years of related experience, with ability to obtain public trust.
We are currently recruiting a Senior Clinical Trials Monitor & Auditor for our team in Bethesda, MD, United States.
We are looking to fill the Senior Clinical Trials Monitor & Auditor position at Dovel Technologies, Inc in Bethesda, MD, United States.
The Senior Clinical Trials Monitor & Auditor role at Dovel Technologies, Inc is now open for applications in Bethesda, MD, United States.
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