GENERAL SUMMARY/ OVERVIEW STATEMENT:
Position available for experienced individual to take lead role in coordinating conduct of multiple studies involving headaches. The successful candidate will work under the general supervision of the Principal Investigator. The CRC1 will take responsibility for conducting the IRB approved research protocols, perform study procedures with subjects, monitor collection of subject data, verify accuracy of study forms, assist with QA/QC audits of data, maintain study regulatory documentation, track deviations, input data, monitor and maintain study equipment, continually review research center work flow for potential efficiency improvements, analyze study proposals and produce operational protocols, and perform additional duties as needed.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assigned to each position.
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