Clinical Research Coordinator II: Trials, IRB & Compliance
Listed on 2026-10-18
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Healthcare
Clinical Research, Medical Science -
Research/Development
Clinical Research, Medical Science, Research Scientist
Tufts Medicine is seeking a Clinical Research professional to support the development of new products and the innovation of clinical trial processes within our research programs.
You will assist the Principal Investigator in planning and implementing clinical studies, coordinating IRB submissions, ensuring HIPAA compliance, and reporting results in line with FDA Good Clinical Practice guidelines, under close supervision.
Are you ready to take on the Clinical Research Coordinator II:
Trials, IRB & Compliance role at Tufts Medicine?
Learn more about the Clinical Research Coordinator II:
Trials, IRB & Compliance role in the description above.
We appreciate your interest in this position.
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This posting is for the Clinical Research Coordinator II:
Trials, IRB & Compliance role at Tufts Medicine, based in Lowell, MA, United States.
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