Nephrology Clinical Research Coordinator

U.S. Renal Care; Toledo (OH); On-site; USD 62,000 - 78,000; Full time

Benefits offered by this job

Medical / Pharmacy

Dental

Vision

Life Insurance

401k with employer match

Virtual Care

PTO

Job summary

U.S. Renal Care in Toledo, OH seeks a Clinical Research Coordinator to support the PI, SCRc, sponsors, CROs, and IRBs to ensure trial execution per protocol and regulatory standards.

You will coordinate participant care from screening through completion, manage informed consent, data entry, and adverse event reporting, while upholding HIPAA and GCP requirements. Travel to investigator meetings and dialysis facilities may be required.

Qualifications

• Bachelor's degree preferred.
• 3 years of clinical research experience required; nephrology experience preferred.
• Basic knowledge of FDA regulations, IRB requirements and Good Clinical Practice (GCP).
• Basic knowledge of kidney care and/or ESRD or similar field is a plus.
• Strong verbal and written communication skills required.
• MS Office and related computer skills; proficiency in USRC applications within 90 days of hire.

Responsibilities

• Coordinate all aspects of participant care from screening through study completion as defined by the protocol and PI delegation.
• Ensure proper informed consent process in line with 45 CFR part 46.
• Maintain and update source records including medical history and documentation of procedures.
• Promptly report adverse events and protocol deviations to the PI and IRB per 21 CFR 312.
• Educate participants on study processes, IP use, safety, and rights.

Skills

Clinical research

Communication skills

MS Office

FDA regulations

IRB requirements

GCP

Nephrology knowledge

USRC applications

Education

Bachelor's degree in related field

Tools

USRC applications

Job description

U.S. Renal Care in Toledo, OH seeks a Clinical Research Coordinator to support the PI, SCRc, sponsors, CROs, and IRBs to ensure trial execution per protocol and regulatory standards.

You will coordinate participant care from screening through completion, manage informed consent, data entry, and adverse event reporting, while upholding HIPAA and GCP requirements. Travel to investigator meetings and dialysis facilities may be required.