Key duties include pre-screening potential participants against protocol eligibility criteria; obtaining and documenting informed consent for non-interventional registry/observational studies and select minimal-risk device studies; assisting with subject enrollment, randomization, and coordination of research visits; reviewing study lab manuals and collecting/processing specimens per protocol; performing accurate data entry from source documents to paper/electronic case report forms (including redaction as requested); and serving as a liaison between research staff and departments where research is conducted, along with other assigned tasks. ''685404'',''true'',''685404'',''false'',''Submission for the position: Clinical Research Assistant - Core-Ctr For Research Excel - (Job Number: 260003WI)'',''false'',''685404'',''false'',''true'',''Clinical Research Assistant - Core-Ctr For Research Excel'',''260003WI'',''!*!