Clinical Research Coord II

Apply now 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: Eastern Daylight Time
Applications close: Eastern Daylight Time

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