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Clinical Research Coordinator I

University of Arizona

Tucson, AZ

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JOB DETAILS
SKILLS
Administrative Skills, Cerner, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Data Entry, File Maintenance, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Informed Consent, Inventory Management, Laboratory Equipment, Order Supplies, Organizational Skills, Record Keeping, Reporting Skills, Research Protocols
LOCATION
Tucson, AZ
POSTED
1 day ago
  • Administer clinical tests and questionnaires as part of clinical research protocols (testing visual acuity, stereoacuity, tear collection, electroretinograms, imaging of retina).
  • Data entry for clinical study protocols and preparation of reports.
  • Prepare documents for submission to Research Intake and IRB, including protocols and consent forms, working with faculty, residents, external sponsors and internal departments.
  • Review daily and weekly patient lists across providers, using Cerner to identify potential study participants. Maintain records of eligibility and participation.
  • Work with patients and families to explain the clinical studies, also involved in the consent process and arrange study follow-up.
  • Assist in research coordination to include administrative support schedule coordination, intake and maintaining records/files.
  • Maintain inventory and lab equipment; order lab supplies.

About the Company

U

University of Arizona

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