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iuvo Clinical is seeking a Contractor Study Startup & Essential Documents Specialist for a six-month engagement to support site start-up activities and Central IRB tasks. The role requires strong regulatory and document management skills within ophthalmology trials.
You will manage essential documents, regulatory trackers, and IRB submissions, coordinating with sites and internal teams to ensure timely activation and compliant TMF. The position is remote in the U.S.
iuvo Clinical is seeking a Contractor Study Startup & Essential Documents Specialist for a six-month engagement to support site start-up activities and Central IRB tasks. The role requires strong regulatory and document management skills within ophthalmology trials.
You will manage essential documents, regulatory trackers, and IRB submissions, coordinating with sites and internal teams to ensure timely activation and compliant TMF. The position is remote in the U.S.