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 eligible patients, discussing studies with families, and obtaining informed consent.
  • The position requires ensuring compliance with Institutional Review Boards (IRB), 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
  • manage IRB submissions and amendments
  • ensure FDA and federal compliance
  • collect and verify clinical data integrity

Nice-to-have

  • collaborate with interdisciplinary research teams
  • participate in grant submission writing
  • develop study plans and case report forms
  • prepare manuscripts and presentations
  • support internal and external quality reviews

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
  • Successful completion of background check
  • Drug screen or physical may be required post-offer

Work Rights

Not specified

Tailored Resume

Cover Letter