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

Org: OP-Ophthalmology

Special Requirements:

Job Family: I-Technical/Professional Research