Clinical Research Coordinator-Hematology

The Ohio State University Wexner Medical Center; Ohio; On-site; USD 55,000 - 85,000; Full time

Job summary

The Ohio State University Wexner Medical Center is seeking a Clinical Research Coordinator in the Hematology division of the Department of Internal Medicine. The position involves coordinating daily clinical research activities, identifying eligible patients, recruiting and enrolling participants, obtaining informed consent, and ensuring compliance with regulatory requirements.

You will assist with data collection and monitoring of patient responses to study treatments.

Qualifications

• Bachelor’s degree in biological sciences, health sciences, social sciences or other medical field or equivalent combination.
• One year experience in a clinical research capacity.
• Knowledge of regulatory and sponsor requirements.
• Experience with Microsoft Office applications.

Responsibilities

• Coordinate daily clinical research activities per approved protocols.
• Identify eligible patients and recruit/enroll participants.
• Obtain informed consent and ensure consent process compliance.
• Assist with data collection, processing, and analysis.
• Monitor patients for adverse reactions and report to appropriate staff.
• Prepare for IRB, FDA, and sponsor audits and reviews.

Skills

Clinical Research

Regulatory Compliance

Communication

IRB Knowledge

Education

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

Tools

Microsoft Office

Data capture systems

Job description

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Job Title: Clinical Research Coordinator-Hematology Department: Medicine | IM Hematology

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 Classical Hematology Division 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.

Minimum Experience Required

One year experience in a clinical research capacity required.

Skills and/or Experience Preferred

Experience or knowledge in inflammatory bowel diseases such as Crohn's; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired.

Required

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 staff are required to be on site. A valid driver's license or reliable transportation will be needed as there may be some travel to other locations in the Columbus Metropolitan Area; those areas include Dublin, Powell, New Albany, Main Campus, and Martha Morehouse Pavillion.

Location

James Cancer Hospital (0375) 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.

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

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