Clinical Research Coordinator
University of ChicagoAbout the role
Department
About the Department
Job Summary
The job performs routine assignments related to scientific research projects. Ensures compliance of research activities with institutional, state, and federal regulatory policies, procedures, directives and mandates. Analyzes possible solutions using standard procedures. May contribute to articles, reports and manuscripts. Assists in drafting presentations on research findings.
Responsibilities
Responsible for data reporting and management, collection of source documents, use and development of case report forms, filing and archiving study records, and resolving data queries.
Under general supervision, collaborating with faculty, clinical staff, support staff, other researchers, residents, and medical students to provide technical and administrative support, as well as development and analysis of both qualitative and quantitative research.
Coordinating study logistics, including participant recruitment, data collection, and data management; drafting study instruments and protocols; assisting in training and protocol development.
Ensuring compliance with institutional and regulatory guidelines.
Assisting in writing and editing research grants and manuscripts.
Designing, implementing and maintaining an active database for data retrieval to ensure study success.
Maintains technical and administrative support for a research project or projects.
Conducts literature reviews. Assists with preparation of reports, manuscripts and other documents.
Maintains general awareness in research techniques or methods, regulatory policies and procedures, and relevant scientific field.
Assisting with administrative tasks for the lab (e.g., taking meeting minutes, scheduling, placing supply orders, managing the lab website and email).
Analyzes and maintains data and/or specimens. Conducts literature reviews. Assists with preparation of reports, manuscripts and other documents.
Maintains recruiting and scheduling research subjects; assisting with developing or amending study protocols; assisting with developing data collection tools; assisting with building databases; and providing general administrative support. Has general awareness in research techniques or methods, regulatory policies and procedures, and relevant scientific field.
Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include a college or university degree in related field.---
Work Experience:
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Certifications:
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Preferred Qualifications
Experience:
Experience in relevant research; experience working in an academic medical center.
Preferred Competencies
Organizational skills.
Problem-solving.
Collaboration.
Attention to detail.
Critical thinking.
Communication skills.
Willingness to learn.
Flexibility.
Working Conditions
Lab environment.
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