The Clinical Research Coordinator III independently manages significant and key aspects of a large clinical trial, or all aspects of one or more small trials or research projects. The role provides guidance to less experienced staff, oversees project data management, and interacts with research participants to address study-protocol issues. It may include supervisory duties and, with appropriate credentialing and training, phlebotomy, specimen collection, or diagnostics. The coordinator supports study operations and compliance by monitoring IRB submissions, responding to requests and questions, interfacing with sponsors and monitors, reporting serious adverse events (SAEs), and resolving study queries. The position also supports study recruitment and retention, audits operations including laboratory procedures, and helps identify and implement corrective actions and process improvements. The coordinator may authorize purchases for supplies and equipment maintenance and assist with grant proposals and protocols. The position is intended to support clinical research. Clinical training requirements must be tracked and monitored through Emory Healthcare under the Clinical Researcher credentialing category. Tasks are generally performed in person at an Emory University location; remote-work days may be granted at department discretion, and Emory may change remote-work status with notice.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Career Level
Senior
Education Level
High school or GED