Clinical Research Coordinator, Comprehensive Cancer Center, Clinical Trials Office at The Ohio State University

Posted in Other 13 days ago.

Location: Columbus, Ohio





Job Description:

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Job Title:Clinical Research Coordinator, Comprehensive Cancer Center, Clinical Trials OfficeDepartment:CCC | Clinical Trials Office


The Clinical Research Specialist 2 coordinates and performs daily clinical research activities in accordance with approved protocols administered by 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






Qualifications




  • 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 (human subjects) 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






Starting Pay: $27.60 hourly



Career Roadmap Mapping:



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

Additional Information:


Additional Information


The OSUCCC - James is the only cancer program in the United States that features a National Cancer Institute (NCI)-designated comprehensive cancer center aligned with a nationally ranked academic medical center and a freestanding cancer hospital on the campus of one of the nation's largest public universities.

Location:James Cancer Hospital (0375)Position Type:RegularScheduled 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 Ohio State University is an equal opportunity employer.



All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability, ethnicity, gender identity or expression, genetic information, HIV/AIDS status, military status, national origin, race, religion, sex, gender, sexual orientation, pregnancy, protected veteran status, or any other basis under the law.



Applicants are encouraged to complete and submit the Equal Employment Identification form.


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