Data Coordinator I

University of Wisconsin Carbone Cancer Center

Madison, WI, US
Base: $23.10 ph (negotiable); bonus/equity: not sp...
**
Accurate clinical trial data entry
Abstract subject data from medical records
Maintain research subject files
** The University of Wisconsin Carbone Cancer Center is seeking a Clinical Trials Data Coordinator I who will be responsible for managing clinical trial data, ensuring accuracy in data entry and reporting, and assisting in maintaining research subject files. The position requires strong communication skills and attention to detail, with opportunities for both remote and in-person work. **

Job Summary

  • The Clinical Trials Data Coordinator will join the Clinical Research Central Office at the University of Wisconsin Carbone Cancer Center to support cancer clinical research within Disease-Oriented Teams.
  • Responsibilities include collecting and abstracting subject data from medical records, resolving data queries, and maintaining accurate research subject charts in compliance with study protocols.
  • The position offers a starting hourly wage of $23.10 along with generous vacation, holidays, sick leave, competitive insurance, and retirement benefits.

Matching Summary

Match Score: 75

** The University of Wisconsin Carbone Cancer Center is seeking a Clinical Trials Data Coordinator I who will be responsible for managing clinical trial data, ensuring accuracy in data entry and reporting, and assisting in maintaining research subject files. The position requires strong communication skills and attention to detail, with opportunities for both remote and in-person work. **

Salary

Base: $23.10 per hour (negotiable); Bonus/Equity: Not specified; Benefits: Generous vacation, holidays, sick leave, competitive insurances, savings accounts, retirement benefits

Skills & Requirements

Must-have

  • accurate clinical trial data entry
  • abstract subject data from medical records
  • maintain research subject files
  • knowledge of Electronic Data Capture systems
  • apply clinical research principles

Nice-to-have

  • excellent communication skills
  • attention to detail
  • training staff experience
  • sponsor monitoring visit coordination

Key Requirements

  • Bachelor's Degree preferred
  • Pass initial caregiver check under Wisconsin Caregiver Law
  • Continuous eligibility to work in the United States without sponsorship

Work Rights

Must have continuous US work eligibility without employer sponsorship

Tailored Resume

Cover Letter