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Clinical Research Coordinator 1

University of Chicago
United Statespart_timeVerifiedPosted 22 Feb 2024

About the role

Department
 

BSD MED - Nephrology - Chapman 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. The CRC1 will be involved with the PI, co-clinical research coordinators and sponsoring agencies to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.

Responsibilities

  • Coordinates all aspects of conducting clinical trials including: screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.

  • Maintains accurate and complete documentation of signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), drug dispensing logs, and study related communication.

  • Plans and coordinates patient schedule for study procedures, return visits, and study treatment schedules.

  • Ensures Standard Operating Procedures (SOP) are implemented and documented in accordance to study sponsor, primary investigator, and regulatory agency specifications. Prepares and maintains protocol submissions and revisions.

  • Educates patients about study procedures to be performed, visit schedule, what to report between and during visits, and potential side effects.

  • Performs assessments at visits and monitors for adverse events.

  • Organizes and attends site visits from sponsors and other relevant study meetings.

  • May recruit and interview potential study patients. May obtain, possess, and transport specimens to appropriate laboratory according to established aseptic techniques.

  • 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.

  • Performs other related work as needed.


Minimum Qualifications
 

Education:

Minimum requirements include vocational training, apprenticeships or the equivalent experience in related field (not typically required to have a four-year degree).

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Work Experience:

Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.

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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 patrons, 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) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.


Job Family
 

Research


Role Impact
 

Individual Contributor


FLSA Status
 

Non-Exempt


Pay Frequency
 

Biweekly


Scheduled Weekly Hours
 

20


Benefits Eligible
 

Yes


Drug Test Required
 

Yes


Health Screen Required
 

Yes


Motor Vehicle Record Inquiry Required
 

No


Posting Statement
 

The University of Chicago is an

Company

University of Chicago

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