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.
#J-18808-LjbffrClinical Trial Documentation Coordinator in Remote at Unknown Company
This position is listed as full time and onsite.