Program Coordinator - Ccc | Clinical Trials Office

The Ohio State University

Columbus, OH, USA
Knowledge of clinical research regulations
Experience in clinical research capacity
Ability to present training programs
The Program Coordinator will promote and ensure ethical research practices within the Clinical Trials Office

Job Summary

  • The Program Coordinator will promote and ensure ethical research practices within the Clinical Trials Office.
  • This role involves developing, coordinating, and presenting trainings related to clinical research conduct.
  • The Ohio State University Comprehensive Cancer Center is dedicated to advancing cancer research and therapies.

Matching Summary

The Program Coordinator will promote and ensure ethical research practices within the Clinical Trials Office.

Skills & Requirements

Must-have

  • Knowledge of clinical research regulations
  • Experience in clinical research capacity
  • Ability to present training programs

Nice-to-have

  • Strong communication skills
  • Experience with software training
  • Ability to develop training assessments

Key Requirements

  • Bachelor's Degree or equivalent
  • One year of clinical research experience
  • Knowledge of good clinical practice guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter