Single Irb Specialist

Mass General Brigham Incorporated

Somerville, MA, United States
Base: $90,000 to $110,000 annually; bonus/equity: ...
Fully remote
Single irb experience required
Reviewing research applications for compliance
Negotiating reliance agreements with external irbs
Mass General Brigham is seeking a Single IRB Specialist for a fully remote role based in Somerville, MA. The position involves liaising with external institutions and ensuring compliance with IRB oversight for multi-site research, requiring extensive experience in clinical research and regulatory affairs

Job Summary

  • The role serves as the primary liaison for investigators relying on external single IRBs and ensures all site-specific institutional requirements are met prior to research activation.
  • Candidates will conduct reviews of applications in compliance with federal, state, and local regulations while coordinating the negotiation of individual study reliance agreements.
  • Mass General Brigham offers competitive base pay ranging from $90,000 to $110,000 annually along with comprehensive benefits and career advancement opportunities.

Matching Summary

Match Score: 85

Mass General Brigham is seeking a Single IRB Specialist for a fully remote role based in Somerville, MA. The position involves liaising with external institutions and ensuring compliance with IRB oversight for multi-site research, requiring extensive experience in clinical research and regulatory affairs.

Salary

Base: $90,000 to $110,000 annually; Bonus/Equity: Not specified; Benefits: Comprehensive benefits, career advancement, differentials, premiums, and bonuses

Skills & Requirements

Must-have

  • Single IRB experience required
  • Reviewing research applications for compliance
  • Negotiating reliance agreements with external IRBs

Nice-to-have

  • Excellent communication and interpersonal skills
  • Ability to work independently and as a team member
  • Experience developing educational workshops

Key Requirements

  • Bachelor's degree required (Master's preferred)
  • 5-7 years of clinical research or regulatory affairs experience
  • CIP credential in good standing or pass within 90 days

Work Rights

Not specified

Tailored Resume

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