Clinical Research Specialist in Regulatory Affairs

2 weeks ago


Cincinnati, Ohio, United States University of Cincinnati Full time
Welcome to the University of Cincinnati

Are you interested in becoming part of a prestigious institution recognized as a leading urban public research university in the United States? The University of Cincinnati, founded in 1819, provides a dynamic campus environment and a legacy of groundbreaking research.

Position Overview

We are seeking a Clinical Research Professional to support regulatory affairs within the Cancer Programs at the College of Medicine, contributing to the University of Cincinnati Cancer Center.

Key Responsibilities
  • Oversee the initiation process for research projects at UC.
  • Assist in feasibility assessments and scientific evaluations.
  • Handle initial IRB applications and regulatory paperwork.
  • Work collaboratively with sponsors, contract research organizations (CROs), and internal teams.
Required Qualifications
  • Bachelor's degree in a relevant discipline.
  • 1-3 years of pertinent experience.
Preferred Qualifications
  • Familiarity with medical and pharmaceutical terminology.
  • Experience in clinical research environments.
  • Excellent communication and organizational abilities.
  • Understanding of FDA regulations and Good Clinical Practice standards.
Work Environment and Physical Requirements
  • Primary function: Sitting

Compensation and Benefits

The University of Cincinnati offers a comprehensive benefits package that includes competitive salaries, insurance options, wellness initiatives, and retirement savings plans.

  • Generous paid time off, tuition remission, and employee discounts are available.

Become a part of the University of Cincinnati, an Equal Opportunity Employer, and engage with our vibrant community.



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