Classification Title: |
Clinical Research Coord II |
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Job Description: |
The UF Health Cancer Center is the 72nd NCI designated cancer center and the only one at a public university in the State of Florida. As a matrix cancer center, we span 11 of the University of Florida's 16 colleges, pulling together a world-class, multi-disciplinary membership of over 330 faculty and 150 staff to address the challenges of the cancer burden faced by the population we serve as we work together to find a cure. As a Study Coordinator II in our Hematologic Malignancies & BMT unit, you will be responsible for the coordination of clinical activities for an assigned portfolio of cancer clinical trials. In this position you will collaborate with other coordinator and research staff, investigators, physicians, nurses and other key personnel in the clinics, hospitals, and at the Cancer Center to ensure compliance with protocol requirements and satisfactory care for patients enrolled in research protocols. In your new role you will be responsible for the following:
This is a professional level position, ideal for candidates interested in furthering their career in clinical research. Employees in these roles operate as part of our collaborative research enterprise and are fundamental to the progress of cancer research being conducted at the University of Florida. A complete job description will be provided to candidates selected for interview. |
Expected Salary: |
$55,000 – $62,500 annually; commensurate with education and experience. This is a TEAMS position, and is eligible for a suite of excellent benefits, retirement options, and paid leave . |
Minimum Requirements: |
Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience. |
Preferred Qualifications: |
Knowledge/Experience:
Qualities:
Skills/Abilities:
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Special Instructions to Applicants: | The University of Florida is committed to non-discrimination with respect to race, creed, color, religion, age, disability, sex, sexual orientation, gender identity and expression, marital status, national origin, political opinions or affiliations, genetic information, and veteran status in all aspects of employment including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Applicants must upload a copy of the following documents to be considered for this position:
Professional clinical research certification (through SOCRA or ACRP) is required at the earliest of 12 months from hire or eligibility. Application must be submitted by 11:55 p.m. (ET) of the posting end date. |
Health Assessment Required: | Yes |
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