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This job was posted by https://illinoisjoblink.illinois.gov : For more information, please see: https://illinoisjoblink.illinois.gov/jobs/11959166 Department

BSD MED - Nephrology - Worcester Research Staff

About the Department

The Section of Nephrology at The University of Chicago is comprised of nineteen faculty members, two Ph.D. scientists, ten postdoctoral fellows as well as a staff of over 20 research, administrative and clinical personnel that are devoted to a mission of excellence in patient care, education and research. The nephrology program is ranked #23 by US News and World Report survey of best hospitals in the United States.

Job Summary

The Clinical Research Coordinator 1 provides support to the faculty of the Section of Nephrology within the Biological Sciences Division.

Responsibilities

• Assist with or plan and implement the clinical study\'s goals and objectives; organize patient enrollment planning; conduct quality assurance activities, compile and analyze data.
• Collect, process, ship & store specimens to appropriate laboratory according to established techniques.
• Coordinate the conduct of the study from startup through closeout, including recruiting, interviewing and & screening of study subjects, obtaining informed consent, collecting research data, & ensuring protocol adherence.
• Plan & coordinate patient schedule for study procedures, return visits, and study treatment schedules.
• Educate patients about study procedures to be performed, visit schedule, data to report between & during visits, and the risks / benefits of the procedures.
• Perform assessments at patient study visits and monitor for adverse events.
• Serve as a resource person to patients on trials.
• Act as a collaborator within the department/unit through improving clinical research practice and serving as a resource.
• Maintain working knowledge of current protocols and internal SOPs.
• Be accountable for high standards of clinical research practice and assist in the development of accountability in others.
• Oversee and participate in the coordination and conduct of complex clinical research studies and ensure compliance with federal and institutional regulations.
• Assist with audits, inspections, and monitoring visits from regulatory agencies or sponsors.
• Provide support to other CRCs and research-related staff, as needed.
• Maintain accurate and complete records which may include -but not limited to- signed informed consents, source documentation, Case Report Forms, and study related communication.
• Prepares for or participates in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
• Participates in study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
• 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.

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Work Experience:

Minimum requirements include knowledge and skills developed through ---

Certifications:

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Preferred Qualifications

Education:

• Bachelor\'s degree.

Experience:

• Knowledge of medical terminology/environment.

Preferred Competencies

• Ability to interact and communicate with clarity, tact, and courtesy with patr ns, patients, staff, faculty, students, and others.
• Strong organizational skills.
• Strong communication skills (verbal and written).
• Excellent interpersonal skills.
• Strong data management skills and attention to detail.
• Knowledge of Microsoft Word, Excel and Adobe Acrobat.
• Ability to understand complex documents (e.g., clinical trials).
• Ability to handle competing demands with diplomacy and enthusiasm.
• Ability to absorb large amounts of information quickly.
• Adaptability to changing working situations and work assignments.

Application Documents

• Resume (required)
• Cover letter (preferred)

When applying, the document(s) MUSTbe uploaded via the My Experience page, in the section titled Application Documents of the application.

Job Family

Research

Role Impact

Individual Contributor

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