Clinical Research Coordinator, Comprehensive Cancer Center, Clinical Trials Office

The Ohio State University Columbus , OH 43216

Posted 2 weeks ago

Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu. 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, Comprehensive Cancer Center, Clinical Trials Office

Department:

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:

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 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.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove

Clinical Research Coordinator, Comprehensive Cancer Center, Clinical Trials Office

The Ohio State University