Overview
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 duties 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.
About Nationwide Children's Hospital
The Behavioral Trials Office (BTO) at Nationwide Children's Hospital works with investigators and research teams throughout the Abigail Wexner Research Institute and Nationwide Children’s Hospital to support our mission of providing efficient coordination of diverse behaviorally-focused clinical research, including behavioral intervention trials (e.g., lifestyle, medication adherence, family communication, biofeedback, safe driving technology) and observational research (e.g., predictors of quality of life, psychosocial outcomes). Our work spans a variety of pediatric departments (e.g., clinical therapies, developmental and behavioral pediatrics, neurology, psychology) and developmental stages (e.g., infancy, adolescence).
