Clinical Research Coordinator B (neurosurgery)

University of Pennsylvania

Philadelphia, Pennsylvania, US
Base: $52,500.00 - $55,000.00 annual rate; bonus/e...
Irb submission and amendment processing
Phase i-iv clinical trial coordination
Adverse event reporting and monitoring
This position independently manages complex phases of clinical trials while ensuring adherence to Good Clinical Practice guidelines

Job Summary

  • This position independently manages complex phases of clinical trials while ensuring adherence to Good Clinical Practice guidelines.
  • The role involves coordinating all regulatory documentation including IRB submissions, adverse event reporting, and study audits by the FDA.
  • Candidates will benefit from a comprehensive benefits package including excellent healthcare, tuition assistance, and generous retirement plans.

Matching Summary

This position independently manages complex phases of clinical trials while ensuring adherence to Good Clinical Practice guidelines.

Salary

Base: $52,500.00 - $55,000.00 Annual Rate; Bonus/Equity: Not specified; Benefits: Comprehensive medical, dental, vision, life insurance, tuition assistance, and retirement plans

Skills & Requirements

Must-have

  • IRB submission and amendment processing
  • Phase I-IV clinical trial coordination
  • Adverse event reporting and monitoring
  • Informed consent administration
  • Source data verification and transcription

Nice-to-have

  • Mentoring coordinators and research assistants
  • Multi-center budget management experience
  • External site monitoring skills
  • Collaboration with sponsors and CROs

Key Requirements

  • Bachelor of Science degree required
  • 2 to 3 years of relevant experience
  • Position contingent upon funding availability

Work Rights

Not specified

Tailored Resume

Cover Letter