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, obtaining informed consent, and assisting with IRB submissions.
  • The position requires ensuring compliance with all Institutional Review Boards, FDA regulations, and industry sponsor requirements.

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 data integrity and reporting
  • collaborate with interdisciplinary teams

Nice-to-have

  • experience writing manuscripts
  • participation in grant submissions
  • ability to analyze complex data
  • strong communication skills with families

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter