Program Coordinator - Ccc | Clinical Trials Office

The Ohio State University

Columbus, Ohio, US
Clinical research practices
Fda regulations
Ich guidelines
The Program Coordinator will serve as a resource to promote and ensure legally compliant and ethical research practices within the Clinical Trials Office (CTO) and Comprehensive Cancer Center (CCC)

Job Summary

  • The Program Coordinator will serve as a resource to promote and ensure legally compliant and ethical research practices within the Clinical Trials Office (CTO) and Comprehensive Cancer Center (CCC).
  • Responsibilities include developing, coordinating, managing, and presenting trainings related to the conduct of clinical research, including FDA Regulations, ICH Guidelines, and NCI requirements.
  • The role involves assisting with staff onboarding, maintaining databases, and acting as a communication center for navigating CTO processes and research updates.

Matching Summary

The Program Coordinator will serve as a resource to promote and ensure legally compliant and ethical research practices within the Clinical Trials Office (CTO) and Comprehensive Cancer Center (CCC).

Skills & Requirements

Must-have

  • clinical research practices
  • FDA regulations
  • ICH guidelines
  • NCI requirements
  • training development and presentation

Nice-to-have

  • strong communication skills
  • collaboration with research teams
  • maintaining databases and SharePoint sites

Key Requirements

  • Bachelor’s Degree or equivalent
  • One year of clinical research experience
  • Knowledge of good clinical practice guidelines
  • Knowledge of federal regulations
  • Computer literacy with Microsoft Office

Work Rights

Not specified

Tailored Resume

Cover Letter