Clinical Research Coordinator-hematology

The Ohio State University

Columbus, Ohio, US
Clinical research protocols
Patient eligibility assessment
Informed consent process
Responsible for the coordination and oversight of clinical research protocols investigating hematology malignancies primarily in observational studies

Job Summary

  • Responsible for the coordination and oversight of clinical research protocols investigating hematology malignancies primarily in observational studies.
  • Coordinates clinical research activities to include identifying and assessing eligibility of patients for clinical research study participation, discussing research studies with patients and their family members, and obtaining informed consent.
  • Ensures that all necessary data is collected and reported as appropriate, and supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA, federal, state and industry sponsor regulations.

Matching Summary

Responsible for the coordination and oversight of clinical research protocols investigating hematology malignancies primarily in observational studies.

Skills & Requirements

Must-have

  • Clinical research protocols
  • Patient eligibility assessment
  • Informed consent process
  • IRB submissions and modifications
  • Data collection and reporting
  • Regulatory compliance

Nice-to-have

  • Manuscript writing
  • Grant submission preparation
  • Interdisciplinary team collaboration
  • Quality assurance reviews

Key Requirements

  • Bachelor's Degree in relevant field
  • 1 year clinical research experience
  • 2-4 years relevant experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter