ical Research Coordinator II
Description
The successful candidate is responsible for managing all of the elements of multiple clinical studies in order to meet all protocol obligations while following ICH/GCP guidelines and departmental/institutional standard operating procedures. These elements include, but are not limited to: start-up activities, launch activities, day to day management of a study, data coding and analysis, report generation, and study closure activities. The CRC II also trains and mentors other clinical research staff to ensure consistency in study management and coordination activities. Previous experience in clinical research or health care field required. Some evening and weekend hours may be required to accommodate data collection efforts. Specific activities may include:
• Participant screening; enrollment; collecting data online, over the phone, and in person; entering data into an electronic database; maintaining participant files and tracking research progress; participant retention activities; creating and maintaining electronic study databases; making recommendations about refinement and/or replacement of study procedures; analyzing operational and outcome related data.
Location: Columbus,
Job Type: Full-time
Contact
Contact: Kelly Boone
Phone: 16147223749
Email: kelly.boone@nationwidechildrens.org
Website: https://external-nationwidechildrens.icims.com/jobs/48277/clinical-research-coordinator-ii—ri-behav-trials-off/job?mode=view&mobile=false&width=1170&height=500&bga=true&needsRedirect=false&jan1offset=-300&jun1offset=-240