Regulatory Coordinator
Regulatory Coordinator
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Under supervision the Regulatory Coordinator will work with the Cancer Center Clinical Trials Office (CC CTO and be responsible for managing all regulatory activities and processing and submitting all documentation related to the Institutional Review Board IRB Research Review Committee RRC Clinical Trials Research Center CTRC and pharmaceutical company regulatory mandates as required for NCI industrysponsored and investigatorinitiated protocols. The Regulatory Coordinator must also maintain credentialing for all Cancer Center partner and contracted affiliate site Investigators and Research Associates through the NCI and related cooperative groups. Duties include monitoring Cooperative Group/Pharmaceutical broadcasts for updates maintaining electronic and paper files for dissemination writing consents facilitating and processing new protocols completing and submitting adverse event forms preparing regulatory records for all site audits and other duties as assigned.
Required Experience:
IC
Employment Type
Full Time
