Posted in Management 30+ days ago.
Type: Full-Time
Responsible for assisting with the facilitation of the Human Research Participant Protection (HRPP) Quality Improvement Program including activities such as study site evaluations, internal monitoring, data collection, quality performance improvement initiatives, coordination, and investigating complaints.
Duties:
Required Education: Bachelor's Degree
Equivalency/Substitution: 48 months related clinical or IRB experience in lieu of the Bachelor Degree for a total of 72 months experience
Skills:
Certifications: Successful completion of the IRB Professional Certification required after two years.
Working Conditions: Standard office environment
Equal Employment Opportunity Statement
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Oklahoma State University-Oklahoma City |
Oklahoma State University-Oklahoma City |
Oklahoma State University-Oklahoma City |