Clinical Research Coordinator - CCC | Clinical Trials Office

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Job Title:
Clinical Research Coordinator - CCC | Clinical Trials Office

Department:
CCC | Clinical Trials Office

Position Summary

The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered by the Recruitment, Intervention and Survey Shared Resource, a part of the Clinical Trials Office within the Comprehensive Cancer Center at The Ohio State University Wexner Medical Center.

Responsibilities

• Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
• Recruit, interview and enroll patients
• Obtain informed consent and ensure consent process is administered in compliance with regulatory and sponsor requirements
• Educate patients and families of purpose, goals, and processes of clinical study
• Coordinate scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with the study protocol
• Assist with monitoring patients for adverse reactions to study treatment, procedure, or medication and notifies appropriate clinical professionals to evaluate patient response, identify the status of complications, & provide the appropriate level of care
• Document unfavorable responses and notify research sponsors & applicable regulatory agencies
• Assist with collecting, extracting, coding, and analyzing clinical research data
• Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state, and industry sponsor regulations
• Assist with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors
• Participate in activities to develop new research protocols and contributes to the establishment of study goals to meet protocol requirements

Job Requirements

Bachelor's Degree in biological sciences, health sciences, social sciences, or other medical field or an equivalent combination of education and experience required. One year of experience in a clinical research capacity is required. Knowledge of medical terminology desired. Clinical research certification from an accredited certifying agency desired. Computer skills required with experience using Microsoft Office Software applications desired. Must be able to effectively communicate, both face-to-face and in writing, with clinical staff, research participants, and outside collaborators.

Additional Information:

As one of only 50 designated comprehensive cancer centers in the nation, The Ohio State University Comprehensive Cancer Center - Arthur G. James Cancer Hospital and Richard J. Solove Research Institute is dedicated to the creation of knowledge in laboratory, clinical and population-based cancer research. We apply those discoveries to develop more effective approaches to cancer prevention, diagnosis, and therapies - providing tomorrow's standard of care today. A Cancer-Free World Begins Here.

Research and Scholarship - Clinical Research - Individual Contributor - Specialized - S2 Experienced

Location:
OSU Gynecologic Oncology (2523)

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.

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