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 legally compliant and ethical research practices within the Clinical Trials Office

Job Summary

  • The Program Coordinator will promote and ensure legally compliant and ethical research practices within the Clinical Trials Office.
  • Responsibilities include developing, coordinating, managing, and presenting trainings related to clinical research.
  • The Ohio State University Comprehensive Cancer Center is dedicated to advancing cancer research and treatment.

Matching Summary

The Program Coordinator will promote and ensure legally compliant and 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