Clinical Research Coordinator- Clinical Trials Management Office
Ohio State University
- # Clinical Research Coordinator- Clinical Trials Management OfficeApplylocations: University Hospitaltime type: Full timeposted on: Posted Todayjob requisition id: R152236Screen reader users may encounter difficulty with this site. For assistance with applying, please contact View email address on click.appcast.io. If you have questions while submitting an application, please review these frequently asked questions.**Current Employees and Students:**If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process.Welcome to The Ohio State University's career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following:* Ensure you have all necessary documents available when starting the application process. You can review the additional job description section on postings for documents that may be required.* Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application.## Job Title:Clinical Research Coordinator- Clinical Trials Management Office## Department:Medicine | Clinical Trials Management Office EarningsClinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Center for Clinical Research Management (CCRM) for the Division of Gastroenterology and Hepatology in the Department of Internal Medicine; 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.**Experience Required**One year experience in a clinical research capacity required.**Desired Experience**Experience or knowledge indiseases of the liver preferred; knowledge of medical terminology desired. Computer skills required with experience using Microsoft Software applications desired.**Certification Desired**Clinical research certification from an accredited certifying agency desired (ACRP or SOCRA).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**CAREER BAND: Individual Contributor-Specialized**CAREER LEVEL: S2*## Additional Information:This is a patient facing role and is required to be on site.Some travel to other OSUWMC Outpatient sites may be required within the Columbus Metropolitan Area. Those locations are Dublin, New Albany, Martha Morehouse, Powell, Outpatient East, and East Hospital.## Location:University Hospital - Doan Hall (0089)## Position Type:Regular## Scheduled Hours:40## **Shift:**First Shift***Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.***Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions.
- J-18808-Ljbffr Ohio State University
Vacancy posted 20 hours ago
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