Medical University of South Carolina
UNIV - Research Program Coordinator II - Department of Medicine: Division of GI
Medical University of South Carolina, Charleston, South Carolina, United States, 29401
Research Program Coordinator II
The candidate will assist the Principal Investigator and research team in the collection of research data, data entry, the recruitment of research participants, and miscellaneous organizational tasks for studies being conducted in the Department of Gastroenterology and Hepatology. The candidate will work primarily on research studies that focus on the study of and development of treatments for nonalcoholic steatohepatitis and other chronic liver diseases. The Research Program Coordinator II will be directly involved in the collection and organization of all study specific data that could include EDC, queries, questionnaires, interviews to assess inclusion/exclusion criteria, laboratory samples as required, and other research related tasks as required per protocol. This role will also provide guidance to the team in regard to Oncore. This position will be responsible for this crucial platform for many complex research studies, including setting up all new studies, maintaining each protocol, and training other staff members how to utilize.
The candidate will assist the Principal Investigator and research team in the collection of research data, data entry, the recruitment of research participants, and miscellaneous organizational tasks for studies being conducted in the Department of Gastroenterology and Hepatology. The candidate will work primarily on research studies that focus on the study of and development of treatments for nonalcoholic steatohepatitis and other chronic liver diseases. The Research Program Coordinator II will be directly involved in the collection and organization of all study specific data that could include EDC, queries, questionnaires, interviews to assess inclusion/exclusion criteria, laboratory samples as required, and other research related tasks as required per protocol. This role will also provide guidance to the team in regard to Oncore. This position will be responsible for this crucial platform for many complex research studies, including setting up all new studies, maintaining each protocol, and training other staff members how to utilize.