Clinical Research Coordinator

As a Clinical Research Coordinator, you will provide support for research studies through the identification, collection, and reporting of clinical trial data. You will compile research, reports and regulatory documents as required by the protocol, and study/sponsor. This involves ensuring research information is timely, accurate, valid, meaningful, and to the sponsor's satisfaction, and that studies are run according to local and global regulations.

Completion of a minimum two year diploma or certificate in a health care related field. Minimum of two years' clinical research experience.

Previous experience in Diagnostic Imaging (minimum 3 years required). Previous experience in Cancer Care. Must be able to work all shifts, as assigned. Must be able to work in Diagnostic Imaging and Nuclear Medicine environment. Proficiency in MS Office applications.

As Required.