Clinical Research Coordinator - Oncology

Ohio State University; Columbus (OH); On-site; USD 52,000 - 76,000; Full time

Job summary

The Ohio State University’s James Cancer Hospital and Solove Research Institute seeks a Clinical Research Coordinator to support oncology trials. You will assist with patient records, consent, data collection, and study coordination across multiple OSU locations.

The role requires a bachelor’s degree in biological or related fields, strong communication, and experience in clinical research; SoCRA/ACRP certification is preferred.

Qualifications

• Bachelor’s Degree in biological sciences or related field required.
• One year of clinical research experience is required.
• Knowledge of medical terminology desired.
• Clinical research certification from SoCRA/ACRP is preferred.
• Computer skills with Microsoft Office applications required.

Responsibilities

• Assist with assessing patient records to identify eligibility for protocols.
• Recruit, interview and enroll patients.
• Obtain informed consent and ensure consent process compliance.
• Educate patients and families about study purpose, goals, and processes.
• Coordinate scheduling of patient visits, procedures and tests per protocol.
• Monitor patients for adverse reactions and report to appropriate clinicians.
• Document unfavorable responses and notify sponsors and regulatory agencies.
• Assist with collecting, extracting, coding, and analyzing research data.
• Support IRB and sponsor regulatory compliance and reviews.
• Prepare for external quality assurance and audits.

Skills

Communication skills

MS Office

Medical terminology

Education

Bachelor’s Degree in biological sciences or related field

Job description

## Clinical Research Coordinator - OncologyApplylocations: James Cancer Hospital and Solove Research Institutetime type: Full timeposted on: Posted 8 Days Agojob requisition id: R153538Screen 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 log in to Workday to use the internal application process.Welcome to The Ohio State University's career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following:* Ensure you have all necessary documents available when starting the application process. You can review the additional job description section on postings for documents that may be required.* Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application.## Job Title:Clinical Research Coordinator - Oncology## Department:CCC | Clinical Trials Office**Position Summary**The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered by the Clinical Trials Office (CTO) within the Comprehensive Cancer Center at The Ohio State University Wexner Medical Center.Applying to this posting will allow you to be considered for multiple Clinical Research Coordinator opportunities within the CCC | Clinical Trials Office. Positions may be available across various locations, including the OSU Main Medical Campus, James Outpatient Care, The Stefanie Spielman Comprehensive Breast Center, Martha Morehouse Outpatient Care, and the Mill Run Gynecologic Oncology Clinic. Specific openings may vary over time, and applicants will be matched to appropriate roles as they become available.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 related 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.As the Clinical Trials Office continues to grow and expand with the opening of new facilities, employees may be required to travel between locations within the greater Columbus region. Flexibility and adaptability are important, as staff may support studies at multiple sites based on operational needs.***The university will not sponsor work visas for this position.***## 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.**Why Join the CTO?** This is a full-time position with a first shift schedule, offering an excellent opportunity to gain hands-on experience in clinical research and build a strong foundation for long-term career growth in the field. The Clinical Trials Office is committed to supporting professional development, including guidance and resources for employees interested in pursuing SoCRA or ACRP certification. Team members also have opportunities to explore career advancement within clinical research operations and regulatory affairs.Additionally, The Ohio State University offers a Master of Clinical Research degree program through the College of Nursing - a valuable option for those looking to deepen their expertise. With OSU’s generous, fully paid tuition assistance program, this combination provides a compelling pathway for career and academic growth.Lastly, the Clinical Trials Office offers staff the opportunity to apply and participate in the OSUCCC Professional Clinical Research Training Academy once a year. The Academy is a year-long program designed to expand knowledge and career potential in clinical research.## 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.