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Clinical Research Regulatory Coordinator
JOB SUMMARYUnder general supervision, promotes and facilitates the regulatory compliance for the division; independently completing a multitude of regulatory responsibilities. The position is responsible for submitting reports, amendments, and continuing review to the IRB; processing approved documents; creating essential study documents for regulatory files and outside sponsors; and creating and auditing all study regulatory documents. The position upholds compliance by developing and exercising procedures to ensure timely document flow (paper and electronic) between the regulatory library, IRB, and outside sponsors.PRIMARY JOB RESPONSIBILITIESWorks collaboratively with leaders, clinicians and other staff in the deve
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