Clinical Research Coordinator - Oud Genomics

The General Hospital Corporation Mass General Brigham

399 Revolution Drive, MA, United States
Base: $20.16 - $29.01phly; bonus/equity: not speci...
Fully remote
Clinical research protocols knowledge
Patient recruitment for clinical trials
Data collection and quality control
Mass General Brigham supports patient care, research, teaching, and community service with a commitment to exceptional care and groundbreaking medical discoveries

Job Summary

  • Mass General Brigham supports patient care, research, teaching, and community service with a commitment to exceptional care and groundbreaking medical discoveries.
  • The Clinical Research Coordinator will assist with regulatory and operational needs for an NIH-funded study on genetic tests for substance use disorders, ensuring high-quality study execution and compliance.
  • The position offers competitive base pay, comprehensive benefits, career advancement opportunities, and a supportive environment recognizing the unique value each team member brings.

Matching Summary

Mass General Brigham supports patient care, research, teaching, and community service with a commitment to exceptional care and groundbreaking medical discoveries.

Salary

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

Skills & Requirements

Must-have

  • clinical research protocols knowledge
  • patient recruitment for clinical trials
  • data collection and quality control
  • regulatory compliance and IRB submissions
  • qualitative and quantitative data analysis
  • study coordination and scheduling

Nice-to-have

  • strong organizational skills
  • excellent communication skills
  • ability to work independently and collaboratively
  • flexibility in work assignments
  • experience with REDCap and EPIC
  • manuscript preparation assistance

Key Requirements

  • Bachelor's degree in related field
  • 0-2 years post-baccalaureate research experience
  • experience with human subjects research and IRB documentation
  • experience recruiting participants in clinical settings
  • experience with qualitative and quantitative data collection
  • ability to provide degree equivalency verification if degree pending

Work Rights

Not specified

Tailored Resume

Cover Letter