Clinical Research Specialist-SMS-3785

Benefits

Qualifications

• •Desktop: Google Chrome, Edge with Chromium
• •Graduate of an accredited college with a minimum of a Bachelor’s Degree
• •Sensitive to the needs of underrepresented minority populations
• •Pre-employment background screenings required
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Responsibilities

• •Provide operational support for clinical research and/or research development activities in the Center for Clinical Research (CCR) and participate in research projects for other Departments, as appropriate
• •This position requires strong interpersonal skills and a basic understanding of the policies and the guidelines that govern clinical research activities
• •A.Provides general support to CCR research staff, coordinators, and/or investigators
• •B.Gathers pertinent research documentation (files, medical records, reports, films, etc) andassists research coordinators and investigators to maintaining research data bases,research source documents and case report forms
• •C.May enter patient data into files and automated research databases
• •D.May collect, verify records, and maintain data on clinical activity and/or research;prepares associated reports as required
• •E.May assist in maintaining patient enrollment folders, consent forms, and supplies
• •F.Develops and maintains a positive working relationship within the CCR, outsidedepartment, hospital personnel, and outside agencies
• •May perform miscellaneous job-related duties as assigned
• •Contact research subjects to coordinate and schedule follow-up visits
• •Provide follow-up to site monitors, IRB personnel, physicians regarding pertinent patient information when necessary
• •J. May be responsible for on call duties
• •Attends mandatory CCR and School of medicine-required meetings, and other work-related educational programs
• •Gather patients’ related information for studies through hospital records; SIU medical records; physician notes and records
• •May perform periodic internal quality assurance audits of study related materials to maintain site readiness for external audits
• •May perform routine laboratory procedures and patients assessments
• •Provides IRB regulatory support to residents and faculty, as directed, including but not limited to preparation of IRB submission materials, development of informed consent documents, maintenance of study approvals
• •Assist or performs project-specific literature searches and/or literature reviews as the directed by faculty
• •May assist in preparing and submission of research abstracts and manuscripts for faculty and resident research projects
• •May assist faculty with the development of materials necessary for regional and/or national presentation of research results
• •May assist faculty with basic data analysis needs
• •Will facilitate statistical support needs for projects using institutional and/or department level statisticians, as directed
• •May assist faculty with submission of internal or external grant applications
• •May order supplies and services required for clinical studies in accordance with the budget and Department/University purchasing guidelines
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