The Clinical Research Coordinator B manages phases of complex clinical trials under general supervision. The Clinical Research Coordinator B will work closely with other study personnel in the University of Pennsylvania’s IBD-Immunology Initiative (I3) study, a prospective clinically annotated biobank, and its related studies, as well as clinical research trials in the IBD Section of the Division of Gastroenterology. Duties related to the I3 and/or related studies will include (but are not limited to) screening of patients; patient consent, enrollment and follow-up; tissue procurement, processing, storage and shipping; data entry; assistance with Institutional Review Board IRB documents; coordination of collaborative studies utilizing the biobank; database management; and coordination with multiple research projects and personnel. Other general duties include (but are not limited to): attending study related meetings; assisting with the preparation of documents needed for initiation, monitoring, and close-out visits with sponsors and/or clinical research organizations; maintenance of appropriate study documentation, case-report forms and study binders; prepares and process all regulatory documents (including those to the University of Pennsylvania Institutional Review Board); maintenance of telephone and/or email and/or mail follow-up with all study patients as directed by protocol and in a timely manner; mailings and other clerical duties; screening of potential patients for research studies and collaboration; scheduling appropriate clinical research study patient appointments; processing and shipping blood, stool and/or tissue specimens for clinical trials; assisting in resolving regulatory-related queries; performance of blood draws or other measurements and testing. The CRC will work closely with the overall research team to accomplish study goals, identify problems and develop solutions. Position contingent upon funding
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Job Type
Full-time
Career Level
Mid Level