Clinical Research Coordinator-Gastroenterology Hepatology and Nutrition

Ohio State University; Columbus (OH); Sur place; USD 42 000 - 60 000; Plein temps

Résumé du poste

Ohio State University seeks a Clinical Research Coordinator for the Gastroenterology, Hepatology and Nutrition division. You will coordinate daily clinical studies, recruit and consent participants, and manage data collection in accordance with approved protocols.

This patient-facing, on-site role is based at University Hospital. Responsibilities include scheduling visits, monitoring safety, and ensuring regulatory compliance with IRB and sponsor requirements.

Qualifications

• Bachelor’s degree required in Biological Sciences, Health Sciences, Social Sciences or related field.
• 1 year of relevant clinical research experience required.
• Preferred: 2–4 years of experience; knowledge of medical terminology; certification in clinical research.

Responsabilités

• Coordinate daily clinical research activities for Gastroenterology/Hepatology/Nutrition studies.
• Identify eligible patients by reviewing records, recruit, interview and enroll participants.
• Obtain informed consent and ensure consent process complies with regulatory and sponsor requirements.
• Schedule and coordinate patient visits, procedures and diagnostic testing per protocol.
• Monitor patients for adverse events and report to appropriate clinical personnel and sponsors.
• Assist with data collection, extraction, coding and analysis; generate reports and ensure data validity.
• Maintain compliance with IRB, FDA regulations and sponsor requirements.

Connaissances

Clinical Research

IRB Compliance

Data Collection

Regulatory Knowledge

Formation

Bachelor's Degree in Biological/Health/Social Sciences or related field

Outils

Microsoft Office

EDC Systems

Description du poste

Clinical Research Coordinator-Gastroenterology Hepatology and Nutrition# Careers## Clinical Research Coordinator-Gastroenterology Hepatology and NutritionApply: University Hospital: Full time: Posted Today: R161662Screen reader users may encounter difficulty with this site. For assistance with applying, please contact [e-mail]. 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-Gastroenterology Hepatology and Nutrition## Department:Medicine | IM Gastroenterology Hepatology and Nutrition**Job Summary:**Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer College of Medicine (COM) Center for Clinical Research Management (CCRM) for the Division of Gastroenterology/Hepatology/Nutrition 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 equivalent combination of education experience required. **Minimum Experience Required**One year of relevant experience required. **Preferred Experience and Skills**2-4 years of relevant experience preferred. Knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired. *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 ResearchCAREER BAND: Individual Contributor- SpecializedCAREER LEVEL: S2## Additional Information:This is a patient facing position and is required to be on site. This position is based from University Hospital. A valid driver's license is required as there will be occasional travel to other OSUWMC outpatient locations such as Outpatient New Albany, Dublin, Powell, Outpatient Care 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.***