Program Coordinator - Ccc | Clinical Trials Office

The Ohio State University

Columbus, Ohio, United States
Knowledge of fda regulations
Experience in clinical research
Training presentation skills
The Program Coordinator will promote legally compliant and ethical research practices within the Clinical Trials Office

Job Summary

  • The Program Coordinator will promote legally compliant and ethical research practices within the Clinical Trials Office.
  • Responsibilities include developing and presenting trainings on clinical research regulations and guidelines.
  • The role involves collaborating with staff to ensure successful onboarding and training completion.

Matching Summary

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

Skills & Requirements

Must-have

  • Knowledge of FDA regulations
  • Experience in clinical research
  • Training presentation skills

Nice-to-have

  • Strong communication skills
  • Ability to collaborate effectively
  • Experience with SharePoint

Key Requirements

  • Bachelor's Degree or equivalent
  • One year of clinical research experience
  • Clinical research certification desired

Work Rights

Not specified

Tailored Resume

Cover Letter