Clinical Research Coordinator-hematology

The Ohio State University

Columbus, OH, US
Coordinate clinical research protocols
Assess patient eligibility for studies
Obtain informed consent from patients
The role involves coordinating and overseeing clinical research protocols investigating hematology malignancies primarily in observational studies

Job Summary

  • The role involves coordinating and overseeing clinical research protocols investigating hematology malignancies primarily in observational studies.
  • Candidates will be responsible for identifying patient eligibility, discussing studies with families, and obtaining informed consent.
  • The position requires ensuring compliance with Institutional Review Boards, FDA regulations, and maintaining strict data integrity.

Matching Summary

The role involves coordinating and overseeing clinical research protocols investigating hematology malignancies primarily in observational studies.

Skills & Requirements

Must-have

  • coordinate clinical research protocols
  • assess patient eligibility for studies
  • obtain informed consent from patients
  • ensure IRB and FDA compliance
  • analyze and verify data integrity

Nice-to-have

  • collaborate with interdisciplinary teams
  • participate in manuscript writing
  • prepare grant submissions
  • develop study plans and case report forms

Key Requirements

  • Bachelor's Degree in Biological or Health Sciences
  • 1 year of relevant Clinical Research experience required
  • 2-4 years of relevant experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter