Job Description

Clinical Research Coordinator – Toledo, OH

Full-Time | Monday–Friday, 9AM–5PM | $65,000–$80,000/year

We’re seeking an experienced Clinical Research Coordinator (CRC) to join a growing research team in Toledo, OH. This role coordinates all aspects of clinical trial conduct—from participant screening through study completion—ensuring protocol compliance, regulatory accuracy, and exceptional patient care.

Key Responsibilities

• Coordinate participant care and study activities in accordance with protocol and GCP guidelines.
• Obtain informed consent and maintain accurate source documentation.
• Report adverse events and deviations per regulatory requirements.
• Dispense and instruct participants on investigational products.
• Manage data entry, resolve queries, and maintain essential study documents.
• Support site visits, audits, and inspections.
• Collaborate with investigators and study teams to ensure quality and compliance.

Qualifications

• Minimum 3 years of clinical research experience
• Experience in a patient-facing research role (CRC, MA, EMT, or Phlebotomist)
• Proven ability to manage multiple industry-sponsored studies
• Working knowledge of GCP, FDA, and HIPAA regulations
• Bachelor’s degree and/or nephrology experience preferred

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