Contributes to the data analysis, reporting, and writing up of results for publication.
Interfaces with research participants, determines eligibility and consents study participants according to protocol for a device clinical trial in a trauma setting at Piedmont Athens Regional Medical Center.
Collects data using the device, directly from the subject, from medical records, and during surgical procedures.
Transcribes data from the data collection forms to electronic case report forms.
Responsible for the management, cleaning, and tracking of the devices. Ensures compliance with research protocols, reviews case report forms and audits for accuracy with source documents, attends monitoring meetings with sponsors.
Prepares regulatory submissions and adverse event reports.
Adheres to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures.
Position entails being on-call including nights and weekends.