"Clinical Research Coordinator"

Under the supervision of a Clinical Research Supervisor or Principal Investigators (PI), the incumbent will perform entry-level duties related to the support and coordination of clinical studies, and may receive training and development to prepare and advance for journey-level work at the next level within the series.

May be responsible for the coordination of one or more single or multi-site, active or follow-up clinical trials; help prepare protocols for study initiation; help design flow sheets, data forms and source documents; gather and interpret medical, surgical and laboratory data regarding clinical trial subjects; may apply understanding of inclusion/exclusion eligibility criteria for protocols; help recruit, enroll, register, schedule and retain study subjects; record protocol specific treatments and assure collection and shipment of samples; assist research personnel to keep patients on study schedules; complete study forms to submit to sponsors and/or appropriate agencies; collect, enter and clean data into study databases, maintaining data quality; assist with data analysis; assist with preparation of reports and tables; attend team meetings; and perform other duties as assigned.

The PI's research lab is in acute need of a Clinical Research Coordinator (CRC) to assist with the currently ongoing study Glaucoma Drainage Device and Endothelial Cell Density Loss Compare (DECLARE) trial, the Clarifying the Optimal Application of SLT Therapy Trial (COAST) trial and other clinical studies. The PI's research lab is in acute need of a CRC to help with the ongoing studies including Pediatric Amblyopia and Strabismus Screening (PASS) study, and the red light for myopia trial. The Pi's work on the Nanodropper for glaucoma trial and Virtual Reality Diagnostic studies together. Due to a nature of the study, The PI needs a person with a sufficient understanding of clinical research, institutional review board, RedCAP database, and coding. In addition, the CRC might assist other faculty in clinical research.

Study description: The DECLARE trial is a multi-center randomized clinical trial to evaluate two different anatomic placements for glaucoma drainage devices and two topical postoperative anti-inflammatory medications with the goal of preventing endothelial cell loss after glaucoma drainage device implantation, with the goal of the study to identify better surgical and medical approaches for glaucoma. The PASS study evaluates the efficacy and cost-effectiveness of two amblyopia screening devices and screening strategies. The red light for myopia trial assess whether low level red light therapy is effective in slowing myopic progression. In addition, the CRC will also take responsibility on other clinical studies. All of these request coding and software engineering to export, convert and manage the data.

The salary range for this position is $34.32 - $55.19 (Hourly Rate).

To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html