Ohio State University
Clinical Research Coordinator - Comprehensive Cancer Center
Ohio State University, Columbus, Ohio, United States, 43215
Clinical Research Coordinator - Comprehensive Cancer Center
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. Research and Scholarship - Clinical Research - Individual Contributor - Specialized - S2 Experienced Location: James Outpatient Care (1043) 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. As required by Ohio Revised Code section 3345.0216, Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion; treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression.
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. Research and Scholarship - Clinical Research - Individual Contributor - Specialized - S2 Experienced Location: James Outpatient Care (1043) 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. As required by Ohio Revised Code section 3345.0216, Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion; treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression.