Clinical Research Coordinator Iii - Pulmonary Medicine

Cincinnati Children's Hospital

Cincinnati, Ohio, United States
Base: $56,784.00 - $62,150.40 annually; bonus/equi...
Full time, day shift
Bachelor's degree in related field
1+ years directly related experience
Good clinical practice (gcp) knowledge
Cincinnati Children's Hospital is seeking a Clinical Research Coordinator III for its Pulmonary Medicine department. The role involves overseeing clinical studies, ensuring compliance with regulatory requirements, and managing participant recruitment and data management

Job Summary

  • The role involves maintaining awareness of active studies and ensuring participant compliance with study protocols and regulations.
  • Candidates will be responsible for recruiting participants, conducting pre-consent screening, and executing the informed consent process according to GCP standards.
  • Cincinnati Children's Hospital is recognized as a top 10 best Children's Hospital and consistently among the top 3 for NIH funding.

Matching Summary

Match Score: 85

Cincinnati Children's Hospital is seeking a Clinical Research Coordinator III for its Pulmonary Medicine department. The role involves overseeing clinical studies, ensuring compliance with regulatory requirements, and managing participant recruitment and data management.

Salary

Base: $56,784.00 - $62,150.40 annually; Bonus/Equity: Not specified; Benefits: Comprehensive benefits package implied

Skills & Requirements

Must-have

  • Bachelor's degree in related field
  • 1+ years directly related experience
  • Good Clinical Practice (GCP) knowledge
  • Regulatory submission preparation
  • Informed consent process execution
  • Case Report Form (CRF) completion

Nice-to-have

  • Master's degree in related field
  • Experience training new staff
  • Ability to problem solve recruitment barriers
  • Collaborative team approach
  • Knowledge of standard operating procedures

Key Requirements

  • Bachelor's degree required OR Master's degree preferred
  • Minimum 1 year of directly related clinical research experience
  • Knowledge of regulatory agencies and human research protocols

Work Rights

Not specified

Tailored Resume

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