Description JOB SUMMARY: Responsible for coordinating the approval processes and conduct of research protocols, such that the integrity and quality of the clinical/translational research is maintained and the research is conducted in accordance within all policies, independently. Responsible for the timely preparation, planning and quality control of regulatory documents required for human subjects research. Supervise set-up and maintenance of biorepositories and assist in manuscript preparation. KEY RESPONSIBILITIES: Submits Informed Consent, Human Subjects' Research Applications, DSMB, HIPAA compliance, Radiation and Biosafety and other pertinent regulatory forms to the IRB for institution approval of clinical trials
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