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Clinical Research Coordinator

The Research Coordinator is charged with protocol execution following good clinical practice guidelines. The Research Coordinator is also responsible for filing study related materials, supply ordering and weekly statistics completion. Interact with, laboratory staff, clinic nursing staff, pharmacy, radiology, office staff and other departments within UCS and outside entities. Assure all study documentation is maintained and accurately completed in a timely fashion. Interact with study sponsors, principal investigators, and sub investigators.
Participate in and facilitate monitoring visits and inspections/audits of the site by the sponsor and/or Federal regulators and has a basic understanding of regulatory processes. Recruit study subjects and assess for eligibility. Discuss study with subject and obtain informed consent; assure study visits and tests are done at appropriate time intervals. Comply with FDA regulations and GCP/ICH guidelines for conducting clinical trials. Patient Registration. Data Compilation. Follow-Up and Maintenance
Incumbent must be organized and pay close attention to detail, possess excellent written and oral communication skills. Must have sound medical terminology and have strong ability to operate a computer with high efficiency. Minimum of 2 years clinical research experience, Oncology preferred. NIH "Human Research Protection" training expected within six weeks.
High School or equivalent required. Bachelor's degree in a health-related science field preferred.
Contact: Carol Dean
Phone: 801-262-9494
Email: cdean@utahcancer.com
Please email your resume to cdean@utahcancer.com. Fax to 801-262-0507 or apply on-line at www.utahcancer.com

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