Clinical Research Coordinator-Cardiovascular Medicine

The Ohio State University Wexner Medical Center; Columbus (OH); Vor Ort; USD 52.000 - 78.000; Vollzeit

Zusammenfassung

The Ohio State University Wexner Medical Center is seeking a Clinical Research Coordinator to coordinate and perform daily clinical research activities in cardiovascular medicine under the Center for Clinical Research Management. You will identify eligible patients, recruit, enroll, obtain informed consent, and ensure regulatory compliance.

You will assist with data collection, sample handling, and reporting, monitor for adverse events, and support quality assurance and IRB submissions.

Qualifikationen

• Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field.
• Minimum 1 year of relevant clinical research experience.
• Preferred 2–4 years of relevant experience and knowledge of medical terminology.
• Clinical research certification (ACRP or SOCRA) desirable; Microsoft Office skills desirable.

Aufgaben

• Coordinate and perform daily clinical research activities per protocol.
• Identify eligible patients, recruit, interview, and enroll.
• Obtain informed consent and ensure consent procedures comply with regulatory and sponsor requirements.
• Assist with collection, processing and evaluation of biological samples and data.
• Monitor patients for adverse events and notify appropriate clinical staff.
• Support IRB, FDA and sponsor regulatory compliance and quality reviews.
• Assist with protocol development and establishment of study goals.

Kenntnisse

Medical terminology

Ausbildung

Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field

Tools

Microsoft Office

Jobbeschreibung

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 Cardiovascular Medicine 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

1 year of relevant experience required.

Preferred Experience

2-4 years of relevant experience preferred.

Preferred Skills and Certification

Knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired (ACRP or SOCRA); 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 Research

CAREER BAND: Individual Contributor- Specialized

CAREER LEVEL: S2

This is a patient facing position and is required to be on site.

Occasional evenings and weekends may be required depending on the approved protocol requirements. Occasional travel may be required within the Columbus Metropolitan Area; locations may be Outpatient Dublin, New Albany, Upper Arlington, Powell, Martha Morehouse, Outpatient East.

Thank you for your interest in working at Ohio State.

Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.

The university is an equal opportunity employer, including veterans and disability.