CLINICAL RESEARCH COORD A
Duties: Coordinates research studies; assists with new clinical study protocols using a wide range of diagnostic and investigative protocols; assists in obtaining initial and amended approvals for protocols; maintains required paperwork and correspondence with the IRB; coordinates data collection; disseminates patient protocol information, monitors patient accrual, protocol adherence; maintains research files; ensures compliance with Good Laboratory Practices (GLP).
Position is contingent on continued funding.
Qualifications: A Bachelor's Degree and 1 year to 2 years of experience or equivalent combination of education and experience is required.
Reference Number: 40-26181
Salary Grade: 025
Employment Type: Exempt
Job Family: I-Technical/Professional Research