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Regulatory Specialist II
We are seeking a Clinical Research Regulatory Specialist II who will be responsible for ensuring that all research studies maintain accurate and up-to-date regulatory files. They will serve as a central resource for faculty conducting clinical research. Working closely with the Program Manager and Research Nurse, this position will complete and submit the initial IRB submission. Prior to the start of a study, will ensure all proper regulatory documents have been approved and that all documents, CRF, databases, monitoring/auditing requirements have been completed. Will produce and maintain a regulatory binder prior to the study starting with all required documents and additional sections for future documents. Works closely with Program Manager to ensure all documents ar


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