Clinical Research Coord III
About The Position
Essential duties: Clinical Trial Project Management Support the Pulmonary Medicine principal investigator with industry sponsored clinical trials or internally funded clinical research. Screen daily/weekly to enroll patients into clinical trial. Coordinate with Clinical Research Center, inpatient unit or inpatient auxiliaries to schedule patients for study visits. Consent patients for enrollment, complete medical history, and document and maintain patient records. Visit frequently with the study monitor to ensure compliance with industry protocol guidelines. Ensure compliance with Divisional research tracking log. Process patient stipends. Prepare and submit reports to the Institutional Review Board in a timely manner. Clinical trial regulatory management Responsible for knowing, implementing, monitoring, and assuming the programs' compliance with regulations and ensuring compliance with UF institutional regulations regards research. Maintain timely, accurate, and thorough records of the program's research activities to fulfill ongoing needs and reporting requirements. Comply with requirements of governing institutions and research sponsors. Write report and maintain research program operation procedures in conjunction with the Principal Investigator. Prepare paperwork needed for study approval. Comply with all institutional, federal, state, sponsor, and departmental policies. Retain records/archive documents after study close-out. This position will perform ad hoc assignments as assigned by the Supervisor
Requirements
- Bachelor's degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.
Responsibilities
- Support the Pulmonary Medicine principal investigator with industry sponsored clinical trials or internally funded clinical research.
- Screen daily/weekly to enroll patients into clinical trial.
- Coordinate with Clinical Research Center, inpatient unit or inpatient auxiliaries to schedule patients for study visits.
- Consent patients for enrollment, complete medical history, and document and maintain patient records.
- Visit frequently with the study monitor to ensure compliance with industry protocol guidelines.
- Ensure compliance with Divisional research tracking log.
- Process patient stipends.
- Prepare and submit reports to the Institutional Review Board in a timely manner.
- Responsible for knowing, implementing, monitoring, and assuming the programs' compliance with regulations and ensuring compliance with UF institutional regulations regards research.
- Maintain timely, accurate, and thorough records of the program's research activities to fulfill ongoing needs and reporting requirements.
- Comply with requirements of governing institutions and research sponsors.
- Write report and maintain research program operation procedures in conjunction with the Principal Investigator.
- Prepare paperwork needed for study approval.
- Comply with all institutional, federal, state, sponsor, and departmental policies.
- Retain records/archive documents after study close-out.
- Perform ad hoc assignments as assigned by the Supervisor
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Industry
Educational Services
Number of Employees
5,001-10,000 employees
