Responsible for the Staff Education and Quality Assurance activities for Sentara System-wide Clinical Research. Accountable that Sentara meets all regulatory recordkeeping requirements for Research. Conducts quality assurance audits, identifies staff training needs based on Compliance and Quality audit findings, and develops educational programs for staff and investigators. He/she will provide day-to-day leadership and supervision for regulatory staff. Ensures consistent and current quality assurance standards and practices are in place and properly executed, while adhering of federal, state and other regulatory standards, requirements, and guidelines. Facilitates and manages the Research Institutional approval process.<br /><br />Qualifications<br /><br /><strong>Education Level</strong><br />Bachelor's Level Degree OR<br />Master's Level Degree<br /><br /><strong>Experience</strong><br />Required: Clinical Research – 5 years, Management – 2 years<br /><br />Preferred: None, unless noted in the "Other" section below<br /><br /><strong>License</strong><br />Required: None, unless noted in the "Other" section below<br /><br />Preferred: Certified Clin Research Prof, Clinical Research Coordinator<br /><br /><strong>Skills</strong><br />Required: <br /><br />Preferred: None, unless noted in the "Other" section below<br /><br /><strong>Other</strong><br />Bachelor's degree required. Master's Degree in related field, Nursing (MSN), Public Health (MPH) preferred. CCRP/CCRC Certification required within one year of eligibility after hire. Five (5) years progressive experience in clinical trials research required. Two (2) years previous manager experience required. Five years experience leading clinical trials may be considered in lieu of management experience.

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