Location: Chicago, IL Job Description: Works on trials directly assigned. Works on industry sponsored trials which provide consistent monitoring/oversight. Assist senior staff maintain high enrolling studies. Accountable for all data management tasks in support of low complexity clinical research studies. Assist with document collection and review in collaboration with Principle Investigator (PI) while maintaining a high degree of confidentiality. Analyzes and organizes study-related documentation, such as protocol worksheets, adverse event reports, institutional review board documents, or progress reports. Assists with various professional, organizational, and operational tasks under direct supervision. Supports quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups. Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples. Performs other related work as needed. Preferred Qualifications Education: Bachelors degree. Experience: Minimal medical/science related education or position. Preferred Competencies Absorb large amounts of information quickly. Adaptability to changing working situations and work assignments. Attention to detail. Interact and communicate (verbal and written) with clarity, tact, and courtesy with patrons, sponsors, staff, faculty, students, and others. Organizational skills. Read and understand complex documents. Time management. Ability to work independently and as part of a team. Application Documents Resume/CV (required) Cover Letter (required) #J-18808-Ljbffr University of Chicago (UC)
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