LeBauer Pulmonary Care, LB-Pulmonix ResearchCITY:
Greensboro, NCJOB DETAILS:
Exempt: Yes | FTE: 1.0 (40 hours/week) | Schedule: Monday-Friday, 7:45am - 4:45pm | On Call: NoJOB SUMMARY:
Lead, coordinate and perform study specific regulatory documentation across multiple studies of different therapeutic areas and phases, in accordance to appropriate regulations, Standard Operating Procedures (SOPs), and study specific protocols/plans and processes. Lead team in problem solving issues of moderate to complex scope.EDUCATION:
Completion of a bachelor's degree plus a minimum of two years closely related clinical and/or research experience
Completion of a master's degree in Public Health, Health Administration or a related area with one year directly related clinical and/or research experienceEXPERIENCE:
An appropriate combination of education and experience.LICENSURE/CERTIFICATION/REGISTRY/LISTING:
Obtain Good Clinical Practice certification within 30 days of hire and maintain without lapse.
Obtain Human Subjects Research certification within 30 days of hire and maintain without lapse.
Regulatory Affairs Certification (RAPS); Clinical Research Coordinator (CCRC); Clinical Research Associate (CCRA) and/or Certified Clinical Research Professional is preferred.
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