Job Description

Clinical Research Coordinator – Toledo (Part-Time, 20-24 hours/week)

Start Date : immediately
Duration : until 30th September 2026

Key Responsibilities

As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:

  • Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
  • Supporting patient screening and enrollment, including handling informed consent and privacy documentation
  • Coordinating logistical activities for study procedures in line with the study protocol
  • Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
  • Managing and shipping biological samples
  • Communicating with study monitors and responding to study-related inquiries...

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