Hiring.Camp

Clinical Research Coordinator - Oncology

Ohio State University

·

Jun 18, 2026

Location
James Cancer Hospital (0375), United States of America
Type
Full-time
Department
Healthcare
Education
Master
Visa
Not sponsored
Source
Workday

Description

Screen reader users may encounter difficulty with this site. For assistance with applying, please contact [email protected]. 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.

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

Skills

WorkdayClinical TrialsFDAPatient CareCompliance

Similar Jobs

30

Clinical Research Coordinator

Evolution Research Group·Little Rock, AR

2d ago

Clinical Research Coordinator

M3USA·Dallas, TX·Onsite

2d ago

Clinical Research Coordinator

Cardiovascular Associates of America·Hialeah, FL·Onsite

3d ago

Clinical Research Coordinator

Creighton University·Omaha, NE·Onsite

3d ago

Clinical Research Coordinator

Facility 238 - Conifer Revenue Cycle Solutions·West Palm Beach, FL·Onsite

3d ago

Clinical Research Coordinator

Northwestern Medicine·Lake Forest, IL

3d ago

Clinical Research Coordinator

Aoncology·Florida Oncology and Hematology, US

4d ago

Clinical Research Coordinator -

Bayfront Health System·WESLEY CHAPEL, FL

5d ago

Clinical Research Coordinator -

Floridamedclinic·WESLEY CHAPEL, FL

5d ago

Clinical Research Coordinator

Mcgill·Montreal Neuro., Canada

5d ago

Clinical Research Coordinator

Yale·Church St South, 2·Hybrid

1w ago

Clinical Research Coordinator

Yale·Church St South, 2·Hybrid

1w ago

Clinical Research Coordinator

Alsglobal·USA - Phoenix, US·Onsite

1w ago

Clinical Research Coordinator

Utaustin·AUSTIN, TX

1w ago

Clinical Research Coordinator

Cardiovascular Associates of America·Columbus, GA·Onsite

1w ago

Clinical Research Coordinator

NURA, PLLC·Edina, MN

1w ago

Clinical Research Coordinator

Oneoncology·East Brunswick, NJ

1w ago

Clinical Research Coordinator

CenExel·Englewood, CO

1w ago

Clinical Research Coordinator

Gehc·OH05-01-Beachwood-Science Park Drive, US

1w ago

Clinical Research Coordinator

Saintlukes·Saint Luke's Hospital, MO

1w ago

Clinical Research Coordinator

Providence Health & Services·Fullerton, CA·Onsite

1w ago

Clinical Research Coordinator

CARE Fertility·Bedford, TX

1w ago

Clinical Research Coordinator

Alcanza Clinical Research·Phoenix Medical Trials - Gilbert, AZ

2w ago

Clinical Research Coordinator

Thermofisher·US - Richfield, MN - 6601 Lyndale Avenue South·Onsite

2w ago

Clinical Research Coordinator

Providence Health & Services·Spokane, WA·Onsite

2w ago

Clinical Research Coordinator

Alcanza Clinical Research·Coastal Carolina Research Center, SC

2w ago

Clinical Research Coordinator

Oneoncology·Fountain Valley, CA

2w ago

Clinical Research Coordinator

Franciscanalliance·IN - Indianapolis, US

2w ago

Clinical Research Coordinator

Genesiscare·NSW-St Leonards-North Shore Health Hub, Australia

2w ago

Clinical Research Coordinator

Massgeneralbrigham·221 Longwood Avenue Boston, US·Onsite

2w ago