Clinical Research Coordinator-hematology

Ohio State University Physicians Inc

Columbus, Ohio, US
Clinical research protocol oversight
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.
  • Collaborates with an interdisciplinary research team and ensures that all necessary data is collected and reported as appropriate.
  • 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 protocol oversight
  • Patient eligibility assessment
  • Informed consent process
  • IRB submissions and modifications
  • Data collection and reporting
  • Ensuring data integrity

Nice-to-have

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

Key Requirements

  • Bachelor's Degree in relevant field or equivalent
  • 1 year of relevant Clinical Research experience
  • 2-4 years of relevant experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter