Clinical Research Data Specialist I

University of Chicago

United States

On-site

USD 50,000 - 65,000

Full time

6 days ago
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Job summary

The University of Chicago's Department BSD MED - Hematology and Oncology is seeking a Clinical Research Data Manager I to support data collection, entry, analysis, and reporting for low-complexity clinical studies. You will help maintain data integrity and contribute to documentation for clinical research conducted across the university.

Responsibilities include data management tasks under supervision, collaborating with PIs, and participating in quality assurance reviews.

Qualifications

  • Education: college or university degree required.
  • Work experience: typically less than 2 years in related field.
  • Certifications: none specified.

Responsibilities

  • Perform data collection, entry, analysis and reporting for low-complexity clinical studies.
  • Maintain data integrity and quality review per standard procedures.
  • Assist with documentation for clinical research conducted by PIs.
  • Handle data management tasks under direct supervision.
  • Collaborate with PI to collect and review documents while maintaining confidentiality.
  • Participate in QA reviews conducted by sponsors or internal groups.
  • Prepare study-related documentation for analysis (protocol worksheets, adverse event reports, IRB documents).
  • Perform other related work as needed.

Skills

Attention to detail
Time management
Organizational skills
Communication
Independent work
Team collaboration
Adaptability
Fast learner

Education

Bachelor's degree

Job description

The University of Chicago's Department BSD MED - Hematology and Oncology is seeking a Clinical Research Data Manager I to support data collection, entry, analysis, and reporting for low-complexity clinical studies. You will help maintain data integrity and contribute to documentation for clinical research conducted across the university.

Responsibilities include data management tasks under supervision, collaborating with PIs, and participating in quality assurance reviews.

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