Clinical Research Coordinator - Radiation Oncology
- The Ohio State University
- Columbus, Ohio
- Full Time
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.
Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Department of Radiation Oncology.
This position will be required to be in the office 5 days per week with a Monday-Friday work schedule. Work locations include The James Cancer Hospital and Stephanie Spielman Comprehensive Breast Center.
Responsibilities:
Research involving registration of patients, scanning and filing study consents, collecting patient data, for the clinical research trials in Radiation Oncology Department.
This will include collection of current study participant information, as well as up keeping and maintenance of already collected patients information over time, to update their outcomes and survival, as well as additional molecular data.
Assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
Recruits, interviews and enrolls patients
Obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements
Educates patients and families of purpose, goals, and processes of research study
Supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations
Assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors
Participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements
Upkeep of regulatory documents for clinical trials.
Collection, processing, transporting of select biological samples for research trials.
Other duties as assigned
Minimum Requirements:
Bachelors Degree in biological sciences, health sciences, or other medical field or an equivalent combination of education and experience required
One year experience in a clinical research capacity experience or knowledge in c linical research required
Knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired
Computer skills required with experience using Microsoft Software applications desired.
Preferred Qualifications:
Interest in medical writing including, but not limited to, grant/protocol development and journal articles (reviews and original research)
Experience using medical record for clinical data abstraction
Experience with database development and management (e.g. RedCap)
Prior medical publication history