Assistant Program Manager

The General Hospital Corporation

Boston, MA, US
Base: $63,252.80 - $102,596.00 annually; bonus/equ...
Fully remote
Clinical research project management
Protocol development and implementation
Regulatory submissions support
Mass General Brigham is a not-for-profit organization committed to advancing patient care, research, teaching, and community service through high-performing teams

Job Summary

  • Mass General Brigham is a not-for-profit organization committed to advancing patient care, research, teaching, and community service through high-performing teams.
  • The Assistant Program Manager will be responsible for day-to-day management of clinical research projects, including protocol creation, regulatory compliance, and communication with multiple stakeholders.
  • The position offers competitive base pay, comprehensive benefits, career advancement opportunities, and a supportive environment that values diversity and inclusion.

Matching Summary

Mass General Brigham is a not-for-profit organization committed to advancing patient care, research, teaching, and community service through high-performing teams.

Salary

Base: $63,252.80 - $102,596.00 annually; Bonus/Equity: Not specified; Benefits: Comprehensive benefits and career advancement opportunities

Skills & Requirements

Must-have

  • clinical research project management
  • protocol development and implementation
  • regulatory submissions support
  • electronic data capture system oversight
  • clinical trial operations compliance
  • staff supervision and training
  • strong organizational and communication skills

Nice-to-have

  • experience with FDA and IRB processes
  • knowledge of ICH/GCP guidelines
  • analytical and problem-solving skills
  • proficiency in Microsoft Office and audiovisual equipment
  • ability to mentor junior staff
  • self-starter with initiative
  • attention to detail and prioritization

Key Requirements

  • Bachelor’s degree required
  • Minimum three years clinical research experience
  • Master’s degree preferred
  • Experience with clinical trial data management
  • Working knowledge of federal regulations
  • Experience with IRB and FDA submissions
  • Ability to work full-time onsite

Work Rights

Not specified

Tailored Resume

Cover Letter