Clinical Research Coordinator-hematology

Ohio State University Physicians Inc

Columbus, OH, USA
Clinical research protocol coordination
Patient eligibility assessment
Informed consent process
The Clinical Research Coordinator is responsible for coordinating clinical research activities focused on hematology malignancies primarily in observational studies within the Division of Hematology

Job Summary

  • The Clinical Research Coordinator is responsible for coordinating clinical research activities focused on hematology malignancies primarily in observational studies within the Division of Hematology.
  • This role involves collaborating with interdisciplinary teams, ensuring data integrity, supporting study plan development, and participating in manuscript and grant writing.
  • Candidates must support compliance with IRB, FDA, federal, state, and industry sponsor regulations and assist with external quality assurance reviews.

Matching Summary

The Clinical Research Coordinator is responsible for coordinating clinical research activities focused on hematology malignancies primarily in observational studies within the Division of Hematology.

Skills & Requirements

Must-have

  • clinical research protocol coordination
  • patient eligibility assessment
  • informed consent process
  • data collection and reporting
  • IRB submissions and compliance
  • collaboration with interdisciplinary teams

Nice-to-have

  • manuscript writing participation
  • grant submission preparation
  • quality assurance and control review
  • data analysis and interpretation
  • external sponsor coordination

Key Requirements

  • Bachelor’s Degree in Biological, Health or Social Sciences
  • 1 year relevant clinical research experience
  • 2-4 years preferred clinical research experience
  • Successful background check
  • Possible drug screen or physical post-offer

Work Rights

Not specified

Tailored Resume

Cover Letter