Clinical Research Coordinator II: Trials, IRB & Compliance
Listed on 2026-10-06
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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.
We are currently recruiting a Clinical Research Coordinator II:
Trials, IRB & Compliance for our team in Lowell, MA, United States.
This is a genuine position to take on the Clinical Research Coordinator II:
Trials, IRB & Compliance role at Tufts Medicine.
As a Clinical Research Coordinator II:
Trials, IRB & Compliance, you will play an important part at Tufts Medicine in Lowell, MA, United States.
We invite applications for the Clinical Research Coordinator II:
Trials, IRB & Compliance position located in Lowell, MA, United States.
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