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 experienceExperience in a patient-facing research role (CRC, MA, EMT, or Phlebotomist)Proven ability to manage multiple industry-sponsored studiesWorking knowledge of GCP, FDA, and HIPAA regulationsBachelor’s degree and / or nephrology experience preferred