Clinical Trials Data Coordinator – Impact & Compliance
Listed on 2026-10-06
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Administrative/Clerical
Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, is seeking a Data Coordinator to support the Study Coordinator in daily data operations for oncology clinical trials in the United States. You will ensure SOPs, GCP, and ICH guidelines are followed while handling source documentation and data queries.
This role emphasizes attention to detail, timely data deadlines, and collaboration with cross-functional teams to maintain study files, track patient visits, and contribute to
For the Clinical Trials Data Coordinator – Impact & Compliance position at McKesson, we are reviewing applications now.
We are looking to fill the Clinical Trials Data Coordinator – Impact & Compliance position at McKesson in Northern, KY, United States.
The Clinical Trials Data Coordinator – Impact & Compliance role at McKesson is now open for applications in Northern, KY, United States.
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