Clinical Research Coordinator Ii - Hematology/oncology

Vanderbilt University Medical Center Cool Springs

Nashville, Tennessee, United States
Not specified; not specified; comprehensive benefi...
Irb proposal preparation and processing
Regulatory compliance with federal regulations
Patient eligibility assessment and enrollment
The role involves coordinating the approval processes and conduct of research protocols to maintain integrity and quality in clinical and translational research

Job Summary

  • The role involves coordinating the approval processes and conduct of research protocols to maintain integrity and quality in clinical and translational research.
  • Vanderbilt University Medical Center is committed to an environment where employees take exceptional pride in their work and never settle for what was good enough yesterday.
  • This position offers the opportunity to make a meaningful impact within Vanderbilt Health, supported by a comprehensive benefits package including health, disability, and retirement offerings.

Matching Summary

The role involves coordinating the approval processes and conduct of research protocols to maintain integrity and quality in clinical and translational research.

Salary

Not specified; Not specified; Comprehensive benefits package including health, disability, retirement, and wellness offerings

Skills & Requirements

Must-have

  • IRB proposal preparation and processing
  • Regulatory compliance with federal regulations
  • Patient eligibility assessment and enrollment
  • Case report form data entry and accuracy
  • Informed consent process management

Nice-to-have

  • Effective communication with diverse stakeholders
  • Experience with Phase I-III clinical trials
  • Ability to work in a collaborative team environment
  • Proactive problem-solving skills for complex issues

Key Requirements

  • Bachelor's degree required
  • 1 year relevant work experience
  • Knowledge of Good Clinical Practice (GCP)

Work Rights

Not specified

Tailored Resume

Cover Letter