Clinical Research Associate

Center for Integration Science

Boston, MA, US
Base: $20.16 - $29.01phly; bonus/equity: not speci...
Hybrid
Maintain study-specific regulatory binders
Submit protocol amendments to irb
Manage adverse event documentation
The position involves ensuring regulatory requirements for clinical trials are met through collaboration with IRBs, sponsors, and federal agencies

Job Summary

  • The position involves ensuring regulatory requirements for clinical trials are met through collaboration with IRBs, sponsors, and federal agencies.
  • Candidates will be responsible for preparing safety reports, revising informed consent documents, and managing source documentation throughout the trial process.
  • Mass General Brigham offers a comprehensive benefits package, career advancement opportunities, and a competitive hourly pay range of $20.16 to $29.01.

Matching Summary

The position involves ensuring regulatory requirements for clinical trials are met through collaboration with IRBs, sponsors, and federal agencies.

Salary

Base: $20.16 - $29.01/Hourly; Bonus/Equity: Not specified; Benefits: Comprehensive benefits, career advancement, differentials, premiums, and bonuses

Skills & Requirements

Must-have

  • Maintain study-specific regulatory binders
  • Submit protocol amendments to IRB
  • Manage adverse event documentation
  • Participate in clinical monitoring visits

Nice-to-have

  • Effective communication with patients
  • Strong attention to detail
  • Ability to recognize data integrity issues

Key Requirements

  • Bachelor's Degree in Related Field
  • 1-2 years research related experience preferred
  • Working knowledge of clinical research protocols

Work Rights

Not specified

Tailored Resume

Cover Letter