Program Coordinator - Ccc | Clinical Trials Office

The Ohio State University

Columbus, OH, USA
Knowledge of fda regulations
Experience in clinical research
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.
  • Responsibilities include developing and presenting trainings on clinical research regulations and guidelines.
  • The role involves tracking training completion and facilitating staff onboarding processes.

Matching Summary

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

Skills & Requirements

Must-have

  • knowledge of FDA regulations
  • experience in clinical research
  • ability to present training programs

Nice-to-have

  • strong communication skills
  • collaborative team player
  • 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