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Clinical Research Coord II

University of Florida

  • Gainesville, Florida
  • 2 days ago

    Highlights

    Maintain consistent communication at regular/frequent intervals with PI and study team, maintain regulatory binders and patient binders as applicable, maintain good working relationships with study staff and Sponsor/Government Agency representatives, assist with monitor/auditor visits, and assist with grant-required progress reports. Miscellaneous Activities – Activities include but are not limited to: completing tasks assigned to complete human subjects research; Satisfying annual competencies as required by the University of Florida and Institutional Review boards; participating in professional development and continuing education.

    Numbers & Facts

    LocationGainesville, Florida
    Websitehr.ufl.edu/_pageup/favicon.ico

    Description

    Classification Title:

    Clinical Research Coord II

    Classification Minimum Requirements

    Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.

    Job Description:

    Incumbent will coordinate research studies with minimal supervision or as part of an assigned team. Incumbent will perform all Clinical Research Coordinator (CRC) Core responsibilities as well as additional responsibilities detailed below for Clinical Research Coordinator II. Assignments for this position include large scale data extraction from electronic medical records, data entry, and IRB compliance. Incumbent will manage projects according to established deadlines, maintain accurate and timely records, maintain consistent communication and assist with the development of manuscripts, grants, protocols and educational materials as needed.

    Perform detailed chart review, review of inclusion/exclusion criteria, input data into Sponsor and/or internal database(s), resolve data queries in a timely fashion, and assist with data clean up and analysis on specific projects as needed.

    Maintain consistent communication at regular/frequent intervals with PI and study team, maintain regulatory binders and patient binders as applicable, maintain good working relationships with study staff and Sponsor/Government Agency representatives, assist with monitor/auditor visits, and assist with grant-required progress reports.

    Complete required trainings on protocols as directed, work on special projects as needed, conduct literature reviews, and create bibliographies as needed.

    Assist with writing, editing, and/or submitting IRBs for new projects and ensure IRB compliance for current projects.

    Miscellaneous Activities – Activities include but are not limited to: completing tasks assigned to complete human subjects research; Satisfying annual competencies as required by the University of Florida and Institutional Review boards; participating in professional development and continuing education.

    Expected Salary:

    $55,000-$60,000

    Required Qualifications:

    Qualifications refer to evidence-based or demonstrated knowledge, skills, abilities, and experiences required for the role. For TEAMS positions the required qualifications should reflect Classification Minimum Requirements.  For Faculty roles, these qualifications may reflect college-specific requirements needed for success the role.

    Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.

    Preferred Qualifications

    2-3 years experience reviewing medical record or clinical data preferred
    1-2 years human subjects research experience preferred
    Experience applying the following regulations and guidelines: Good Clinical Practice Guidelines, Health Information and Accountability Act (HIPAA), Protection of Human Research Subjects
    Experience using Epic preferred
    Experience working in Electronic Data Capture (EDC) systems preferred
    Able to work collaboratively, forward ideas as appropriate and problem solve when needed.
    Multi-media capabilities strongly preferred; proficiency with Microsoft Office such as Word, PowerPoint and Excel.

    Special Instructions to Applicants:

    In order to be considered, you must upload your cover letter and resume. 

    Application must be submitted by 11:55 p.m. (ET) of the posting end date.

    Health Assessment Required:No.

     

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