Intake & Consenting Coordinator
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Job no: 534404
Work type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Grant or Research Administration, Medicine/Physicians
Department:27300100 - HA-FIXEL ADMINSTRATION
| Classification Title: |
Clinical Research Coord I
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| Job Description: |
Responsible for consenting patients according to the IRB-approved protocol for our databank. Responsible for gathering demographics and entering the participant and certain data into the database.
Incumbent will lead the responsibility in establishing the schedule to facilitate efficient consenting of patients in a busy neurological clinic. Incumbent will communicate needed information to clinic staff to facilitate consenting process as well. Responsible for developing standard operating procedures for various consenting scenarios. Position will require consistent communication with PI, Data Manager, Clinic Faculty, Leadership and Staff. Provide general support for the Data Lab team & Clinic Staff.
Attend Data Lab meetings & Clinic business meetings to discuss consenting duties.
Additional tasks as needed.
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| Expected Salary: |
$46,000 - $50,000
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| Minimum Requirements: |
Associate’s degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.
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| Preferred Qualifications: |
Bachelor’s degree in relevant field.
Experience consenting patients for research.
Knowledge and experience in IRB protocols.
Ability to prioritize and effectively communicate verbally and in writing.
Computer competency including proficiency in Microsoft Word and Excel.
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| Special Instructions to Applicants: |
Please upload the following - CV or Resume, Cover Letter and List of Professional References.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
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| Health Assessment Required: |
No |
Advertised: Eastern Standard Time
Applications close: Eastern Standard Time
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