$ cat jobs/clinical-research-coordinator-supportive-care-comprehensive-the-ohio-state-university-570c64f5a387.json
Clinical Research Coordinator - Supportive Care, Comprehensive Cancer Center
Screen reader users may encounter difficulty with this site. For assistance with applying, please contact . 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 - Supportive Care, Comprehensive Cancer Center Department: CCC | Palliative Medicine Position Summary The Clinical Research Coordinator (CRC) serves as a lead resource for the coordination and execution of clinical research activities within the Center for Research Excellence in Supportive Care (CREST) at the James Cancer Center/Solove Research Institute and the Section for Pain and Palliative Care Research (SPARC) in the Division of Palliative Medicine. CREST focuses on supportive care research in areas such as aging and cognitive impairment, pain and symptom management, substance use, and medical cannabis in individuals with serious illness, particularly cancer. The CRC works closely with principal investigators and research teams to lead, coordinate, and independently manage clinical research studies in compliance with institutional, regulatory, and federal guidelines, including participant recruitment, informed consent, data collection, protocol implementation, preparation and maintenance regulatory documenta