Senior Clinical Research Coordinator - CCC | Clinical Trials Office

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.

reputed company Employees and reputed company:

If you are currently employed or enrolled as a student at reputed company, please log in to reputed company to use the internal application process.

Welcome to reputed company'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 reputed company necessary documents available reputed company starting the application process. You can review the additional job description reputed company 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:

Department:

Position Summary

Senior Clinical Research Coordinator serves as reputed company resource in the execution of assigned clinical research studies in accordance with approved protocols administered by the Clinical Trials Office (CTO) Multi-Center Trial Program (MCTP); oversees & coordinates conduct of daily activities of research studies; serves as primary reviewer of subsite patient records to assess and identify patients who meet criteria for participation in research studies;  ensures informed consent authorization is obtained & administered in compliance to regulatory & sponsor requirements; oversees the collection, processing & evaluation of biological samples, as well as follow-through of patient care appointments, procedures, & other diagnostic testing; monitors subsite patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & reputed company appropriate level of care; ensure the site documents unfavorable responses and notifies research sponsors & applicable regulatory agencies; participates in extracting, coding, and analyzing clinical research data; assists with activities to ensure compliance with Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; participates in planning, organizing and preparing for external compliance and quality assurance and control reviews; actively participates in internal quality assurance audits; participates in development of new research protocols and contributes to planning of goals to meet study requirements; assists with preparation and submission of publications, research reports, and grant proposals.

Job Requirements

Bachelor’s Degree in biological sciences, health sciences or medical field or an equivalent combination of education and experience required; three to five years experience in a clinical research reputed company conducting clinical research studies required; experience in a progressively responsible management reputed company in a medical research environment preferred; experience or knowledge in specialty area preferred; clinical research certification from an accredited certifying agency required; computer skills required with experience using reputed company Software applications desired.

Additional Information:

Location:

Position Type:

Scheduled Hours:

Shift:

Final candidates are subject to successful completion of a background reputed company.  A drug screen or physical may be required during the post offer process.

Thank you for your interest in positions at reputed company and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be reputed company by visiting the Candidate Home reputed company 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.