Job Details

Clinical Research Coord II

Job no: 535505
Work type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Health Care Administration/Support
Department:29090100 - MD-PEDS-ADMINISTRATION

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:

• 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:
$53,000- $59,800

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

Preferred:

• 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:Yes

Advertised: 10 Apr 2025 Eastern Daylight Time
Applications close: 27 Apr 2025 Eastern Daylight Time

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