Clinical Research Coordinator 1 - Cgmp Core

University of Chicago

Chicago, IL, US
Base: $50,000.00 - $65,000.00; bonus/equity: not s...
Cgmp cleanroom environment experience
Aseptic preparation of cellular products
Environmental monitoring and particle counts
The primary mission is to manufacture cell-based products and clinical grade reagents for Phase I, II, and III clinical trials in an FDA-registered cGMP facility

Job Summary

  • The primary mission is to manufacture cell-based products and clinical grade reagents for Phase I, II, and III clinical trials in an FDA-registered cGMP facility.
  • Candidates must adhere to sponsored clinical trial protocols, maintain strict compliance with federal regulations, and perform aseptically prepared cellular infusion procedures.
  • The University of Chicago offers a wide range of benefits programs including health, retirement, and paid time off for eligible employees.

Matching Summary

The primary mission is to manufacture cell-based products and clinical grade reagents for Phase I, II, and III clinical trials in an FDA-registered cGMP facility.

Salary

Base: $50,000.00 - $65,000.00; Bonus/Equity: Not specified; Benefits: Health, retirement, and paid time off included

Skills & Requirements

Must-have

  • cGMP cleanroom environment experience
  • aseptic preparation of cellular products
  • environmental monitoring and particle counts
  • strict adherence to FDA regulations
  • batch record and SOP execution

Nice-to-have

  • ability to work off hours and weekends
  • collaborative team atmosphere skills
  • proficiency with Microsoft Office Suite
  • experience with equipment validation IQOQPQ
  • strong interpersonal communication skills

Key Requirements

  • Bachelor's degree in related field
  • Less than 2 years of work experience required
  • Graduate degree strongly preferred
  • Ability to pass rigorous cGMP training
  • Must be able to lift up to 30 pounds

Work Rights

Not specified

Tailored Resume

Cover Letter