Clinical Research Associate - Regulatory & IRB (Hybrid)

Mass General Brigham; Boston (MA); Hybrid; USD 28,000 - 40,000; Full time

Job summary

Mass General Brigham in Boston seeks a Clinical Research Associate to ensure regulatory requirements for clinical trials are met. You will work with IRBs, sponsors, and federal agencies, and support the trial lifecycle with documentation and reporting.

The role requires a Bachelor’s degree and attention to detail, with hybrid work options and ongoing training in institutional and federal regulations governing clinical research.

Qualifications

• Bachelor's degree required with knowledge of clinical trial processes.
• Ability to recognize compliance and data integrity issues.
• Understanding of IRB processes and federal regulations.

Responsibilities

• Maintain and organize study-specific regulatory binders.
• Prepare protocol amendments, continuing reviews, and safety reports to IRB.
• Revise informed consent documents with new risk information.
• Collect, complete, and submit essential regulatory documents to regulatory entities.

Skills

Attention to detail

Regulatory compliance

Communication skills

Knowledge of clinical research

Education

Bachelor's Degree

Job description

Mass General Brigham in Boston seeks a Clinical Research Associate to ensure regulatory requirements for clinical trials are met. You will work with IRBs, sponsors, and federal agencies, and support the trial lifecycle with documentation and reporting.

The role requires a Bachelor’s degree and attention to detail, with hybrid work options and ongoing training in institutional and federal regulations governing clinical research.