Qualifications Bachelor's degree in a scientific or related field with At least 3 years or CRCI or equivalent clinical research experience [Note: a combination of equivalent education and experience will be considered] Working knowledge of the federal regulations and federal agencies, including the Food and Drug Administration (FDA) and the Office for Human Research Protections (OHRP), as well as familiarity with the International Conference on Harmonisation Guideline for Good Clinical Practice (ICH GCP) Strong organizational, critical thinking, and problem-solving skills Working knowledge of clinical trials contracting and budgeting, including understanding of Medicare Coverage Analysis (MCA) and clinical trials billing compliance, both industry and non-industry Excellent demonstrated interpersonal, verbal, and written communication skills Strong proficiency in Microsoft, Google, data capture systems, electronic medical records, and other computer applications Preferred qualifications Experience with OnCore (Clinical Trials Management System). Job Overview The Clinical Research Coordinator II (CRCII) is the lead coordinator on multiple transplant (liver, kidney, pancreas, bowel) and GI clinical research studies, responsible for the implementation of their assigned portfolio of studies, including but not limited to regulatory submissions, data abstraction/entry/management, participant screening and enrollment, and study management.