Clinical Research Coordinator-Cardiovascular Medicine

The Ohio State University; Davis (CA); On-site; USD 65,000 - 90,000; Full time

Job summary

The Ohio State University seeks a Clinical Research Coordinator for Cardiovascular Medicine at the Davis Heart and Lung Research Institute. This on-site role coordinates daily research activities, screens and enrolls patients, obtains consent, and ensures protocol compliance within IRB, FDA, and sponsor requirements.

Responsibilities include data collection and analysis, scheduling procedures and testing, monitoring adverse events, and contributing to protocol development.

Qualifications

• 1 year of relevant clinical research experience required.
• Bachelor’s degree in a biological/health-related field required.
• Knowledge of medical terminology desired; clinical research certification preferred (ACRP or SOCRA).
• Computer skills with Microsoft software applications required.

Responsibilities

• Coordinate and perform daily clinical research activities per approved protocols.
• Identify eligible patients by reviewing records and recruit/enroll participants; obtain informed consent.
• Educate patients and families about study purpose, goals, and procedures.

Skills

Medical terminology

ACRP Certification

SOCRA Certification

Microsoft Office

Education

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

Tools

Microsoft Office

Job description

Screen 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 l og in to Workday to use the internal application process.

Job Title

Clinical Research Coordinator-Cardiovascular Medicine

Department

Medicine | IM Cardiovascular Medicine

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

Additional Information

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.

Location

Davis Heart and Lung Research Institute (0113)

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.

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