Clinical Research Coordinator-Float

Clinical Research Coordinator-Float page is loaded## Clinical Research Coordinator-Float locations:
Dodd Rehabilitation Hospital time type:
Full time posted on:
Posted Todayjob requisition :
R144690

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Job Title:

Clinical Research Coordinator-Float## Department:

Medicine | Clinical Trials Management Office Earnings Clinical Research Coordinator
- Float to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the College of Medicine (COM) Center for Clinical Research Management (CCRM) in various COM Departments and Divisions conducting non-oncology human subjects research; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients;

obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with study protocol; participates in the collection, processing & evaluation of biological samples; administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires*;
* assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & applicable regulatory agencies; participates in evaluating patients for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data;

generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements.
** Minimum Education Required
** Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required.
** Minimum Experience Required
** One year experience in a clinical research capacity required. Computer experience required.
** Experience Preferred
** Experience or knowledge in coordinating clinical trials preferred; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired. Experience using Microsoft applications desired and knowledge of data base systems such as Red Cap, Medidata, Rave, etc.
* Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen.
** FUNCTION/SUBFUNCTION:
Research and Scholarship/Clinical Research
**…