Job Description
General Summary
Under limited supervision, coordinates and leads the activities of staff engaged in research. Responsible for overseeing research projects, and ensuring that clinic personnel are aware of study protocols. Responsible for day to day operations including assisting with budgets, grant proposals, hiring and disciplinary actions. Schedules staff to maximize efficiency. Acts as a resource for the Research Coordinators and Investigators.
Principal Responsibilities and Tasks
The following statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all job duties performed by personnel so classified.
· Screens patients for eligibility to enter research studies. Ensures that diagnostic tests required for entry to a study are ordered and performed. Assists physicians and/or principal investigators in obtaining informed consent.
· Conducts patient/family education concerning clinical studies.
· Follows the clinical course of patients entered on clinical research studies by obtaining results of diagnostic studies, assessing patients for complications, and recording patient data onto study forms.
· Independently or in collaboration with the departmental research technician, obtains, processes, and ships clinical samples from patients in accordance to protocol guidelines
· Records pertinent patient information on flow sheets and other case report forms and delegates these tasks to data management staff when appropriate.
Qualifications
Education and Experience
Knowledge, Skills and Abilities
Additional Information
All your information will be kept confidential according to EEO guidelines.
Compensation
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