Program Coordinator

Brigham and Women's Faulkner Hospital

Boston, MA, United States
Base: $19.81 - $28.30phly; bonus/equity: not speci...
Hybrid
Irb protocols and regulatory approvals
Grant budgets and submission
Administrative oversight
The Program Coordinator will assist in performing a range of administrative responsibilities for a portfolio of clinical and research projects, including developing and maintaining IRB protocols and grant submissions

Job Summary

  • The Program Coordinator will assist in performing a range of administrative responsibilities for a portfolio of clinical and research projects, including developing and maintaining IRB protocols and grant submissions.
  • This hybrid position involves working with a multidisciplinary team of psychology, social work, psychiatry, and primary care teams to support trauma-informed population mental health interventions for children and families.
  • The role requires strong interpersonal, organizational, and team-oriented skills, with a demonstrated ability to work collaboratively and communicate effectively in a hospital-based setting.

Matching Summary

The Program Coordinator will assist in performing a range of administrative responsibilities for a portfolio of clinical and research projects, including developing and maintaining IRB protocols and grant submissions.

Salary

Base: $19.81 - $28.30/Hourly; Bonus/Equity: Not specified; Benefits: Comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable

Skills & Requirements

Must-have

  • IRB protocols and regulatory approvals
  • grant budgets and submission
  • administrative oversight
  • human subjects research
  • clinical trials and observational studies
  • trauma-informed interventions

Nice-to-have

  • strong interpersonal skills
  • team-oriented skills
  • respectful and professional manner
  • interest in child and family mental health

Key Requirements

  • Bachelor's Degree Related Field of Study required
  • 3+ years of directly related clinical research work experience
  • At least one-year prior clinical research experience interacting with the medical system
  • Experience with developing and managing IRB protocols
  • Experience with grant budgets and data management
  • CITI/ MGB Human Subjects training required

Work Rights

Not specified

Tailored Resume

Cover Letter