Clinical Research Coordinator 1

Georgetown University

Washington, DC, USA
Base: $20.16 - $31.30; bonus/equity: not specified...
On-campus
Good clinical practice (gcp) guidelines adherence
Human subject protection regulations compliance
Hipaa patient confidentiality requirements
Georgetown University is seeking a Clinical Research Coordinator 1 for its Clinical Trials Office, focusing on oncology clinical trials. The role involves coordinating various aspects of clinical research, ensuring compliance with regulations, and working closely with study teams and participants

Job Summary

  • This position serves as a Clinical Research Coordinator 1 responsible for the overall coordination of assigned phase I, II, and III oncology clinical trials at the Lombardi Comprehensive Cancer Center.
  • The role requires strict adherence to Human Subject Protection regulations, HIPAA requirements, and Good Clinical Practice guidelines while managing patient safety and protocol integrity.
  • Georgetown University offers a comprehensive benefit package including medical, dental, vision, disability, life insurance, retirement savings, and tuition assistance.

Matching Summary

Match Score: 85

Georgetown University is seeking a Clinical Research Coordinator 1 for its Clinical Trials Office, focusing on oncology clinical trials. The role involves coordinating various aspects of clinical research, ensuring compliance with regulations, and working closely with study teams and participants.

Salary

Base: $20.16 - $31.30; Bonus/Equity: Not specified; Benefits: Medical, dental, vision, disability, life insurance, retirement savings, tuition assistance

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) guidelines adherence
  • Human Subject Protection regulations compliance
  • HIPAA patient confidentiality requirements
  • Informed consent documentation and collection
  • Serious adverse event reporting protocols
  • Clinical Trials Management System (CTMS) usage

Nice-to-have

  • Ability to work independently and as a team member
  • Strong attention to detail and prioritization skills
  • Experience with oncology clinical trial lifecycle
  • Proactive patient communication and symptom management
  • Collaboration with diverse hospital staff and physicians

Key Requirements

  • Bachelor's Degree in scientific or health related field
  • Two years of related experience in clinical research preferred
  • On-Campus work mode designation required

Work Rights

Not specified

Tailored Resume

Cover Letter