Program Coordinator - Ccc | Clinical Trials Office

The Ohio State University

Columbus, Ohio, USA
Clinical research practices
Fda regulations
Ich guidelines
The Program Coordinator will promote and ensure legally compliant and ethical research practices within the Clinical Trials Office (CTO) and Comprehensive Cancer Center (CCC) by developing, coordinating, managing and presenting trainings related to the conduct of clinical research

Job Summary

  • The Program Coordinator will promote and ensure legally compliant and ethical research practices within the Clinical Trials Office (CTO) and Comprehensive Cancer Center (CCC) by developing, coordinating, managing and presenting trainings related to the conduct of clinical research.
  • Responsibilities include presenting trainings on general research topics, assisting with training on software systems, and organizing and presenting at the CTO PI Orientation.
  • The role involves developing assessments, providing feedback to research staff, and facilitating key aspects of staff onboarding and offboarding.

Matching Summary

The Program Coordinator will promote and ensure legally compliant and ethical research practices within the Clinical Trials Office (CTO) and Comprehensive Cancer Center (CCC) by developing, coordinating, managing and presenting trainings related to the conduct of clinical research.

Skills & Requirements

Must-have

  • clinical research practices
  • FDA regulations
  • ICH guidelines
  • NCI requirements
  • training presentation
  • staff onboarding

Nice-to-have

  • collaboration with stakeholders
  • communication center
  • database management
  • SharePoint management

Key Requirements

  • Bachelor’s Degree or equivalent experience
  • One year clinical research experience
  • Knowledge of good clinical practice guidelines
  • Knowledge of federal regulations
  • Computer literacy
  • Clinical research certification desired
  • Experience presenting training programs desired

Work Rights

Not specified

Tailored Resume

Cover Letter