Clinical Trial Documentation Coordinator
Listed on 2026-09-22
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Healthcare
Healthcare Compliance -
Administrative/Clerical
Caris Life Sciences is seeking a Clinical Study Documentation Specialist to support Caris-sponsored studies and collaborative pharmaceutical research. You will ensure study documents are current, complete, and compliant, coordinating IRB submissions and maintaining trial documentation.
You will liaise with internal teams, sites, IRBs, and sponsors to facilitate timely regulatory submissions, track progress in CTMS, and support site onboarding throughout the trial lifecycle.
Are you ready to take on the Clinical Trial Documentation Coordinator role at Caris Life Sciences?
The following position is for a Clinical Trial Documentation Coordinator with Caris Life Sciences.
Our team is growing, and we are hiring a Clinical Trial Documentation Coordinator in United States.
This Full Time position is for the Clinical Trial Documentation Coordinator role at Caris Life Sciences.
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