Clinical Research Coord III
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Job no: 536186
Work type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Office/Administrative/Fiscal Support, Grant or Research Administration, Health Care Administration/Support
Department:29050903 - MD-PULMONARY-OTHER
| Classification Title: |
Clinical Research Coordinator III
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| Classification Minimum Requirements: |
Bachelor's degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.
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| Job Description: |
The Department of Medicine, Division of Pulmonary is seeking a full time Clinical Research Coordinator III. This position will function independently in a clinical research setting and will be responsible for the complete coordination of assigned clinical research activities. The incumbent may have supervisory responsibilities and must demonstrate effective problem solving, writing and communication skills. The incumbent will lead clinical trials/clinical research within the Division of Pulmonary, Critical Care & Sleep Medicine and ensure compliance with federal, state and university policies.
Essential Functions;
- Clinical Trial Project Management
Support the Alpha-1 Research Laboratory under the direction of Dr. Karina Serban with industry sponsored clinical trials or internally funded clinical research. Screen daily/weekly to enroll patients into clinical trials. Coordinate with Clinical Research Center, inpatient unit or inpatient auxiliaries to schedule patients for study visits. Visit frequently with the study monitor to ensure compliance with industry protocol guidelines. Process patient stipends. Assist the Associate Program Director with any internal/external audits. Attend industry sponsored investigator meetings to gather updates on protocol changes, upcoming amendments, etc. Respond to any new industry sponsored solicitations. Regularly review research study billing to ensure compliance.
- Clinical trial regulatory management
Prepare all CRH paperwork needed for study startup approval. Prepare IRB paperwork needed for study startup. Obtain CRH or IRB approval related to amendments, protocol changes, etc. Comply with all institutional, federal, state, sponsor and Divisional policies. Retain records/archive documents after study close out
- Clinical Trials budget
Assist Dr. Serban with industry sponsored budget proposals. Obtain cost of services for all procedures, study visits, etc. related to trial.
- This position will perform ad hoc assignments as assigned by the Supervisor
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| Expected Salary: |
$53,000 - $76,500 Annually
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| Required Qualifications: |
Bachelor's degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.
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| Preferred: |
Five years of relevant Pulmonary clinical trial experience. Certified in Spirometry. Regulatory IRB and/or nursing degree a plus.
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| Special Instructions to Applicants: |
In order to be considered, you must upload your resume.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
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| Health Assessment Required: |
Yes |
Advertised: Eastern Daylight Time
Applications close: Eastern Daylight Time
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