Nephrology Clinical Research Coordinator

U.S. Renal Care, Inc.; San Antonio (TX); On-site; USD 54,000 - 75,000; Full time

Benefits offered by this job

Medical / Pharmacy

Dental

Vision

Voluntary benefits

401k with employer match

Virtual Care

Life Insurance

PTO

Job summary

U.S. Renal Care, Inc. seeks a Clinical Research Coordinator to support daily trial activities and coordinate participant care from screening to study completion. You will ensure informed consent processes comply with 45 CFR part 46 and maintain source records across multiple sites.

Join a team that adheres to FDA, ICH, and GCP guidelines, protects participant safety, and collaborates with investigators, sponsors, CROs, and IRBs. Prior nephrology experience is preferred.

Qualifications

• Bachelor's degree in related field preferred.
• 1–3 years of clinical research experience required; nephrology experience preferred.
• Basic knowledge of FDA regulations, IRB requirements and Good Clinical Practice.
• Basic knowledge of kidney care and/or End-Stage Kidney Disease (ESKD) or similar field is a plus.
• Strong verbal and written communication skills required.
• Must have intermediate computer skills, including Microsoft Office; proficiency in USRC applications required 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 and document informed consent in accordance with 45 CFR part 46.
• Assist in maintaining each study participant's source records and documentation of procedures.
• Promptly report adverse events, protocol deviations and unanticipated problems to the PI, Sponsor and IRB.
• Provide protocol-based study subject education on all processes including IP use and safety.
• Exchange participant information with the PI and study team for patient safety.
• Maintain HIPAA privacy and protect confidentiality at all times.
• Dispense, administer and instruct on IP use per the protocol and PI direction.
• Collaborate with the clinical team to ensure compliance with the study protocol.

Skills

Verbal & written comm

MS Office

USRC applications

FDA regulations

Clinical research

Education

Bachelor's degree

Job description

U.S. Renal Care, Inc. seeks a Clinical Research Coordinator to support daily trial activities and coordinate participant care from screening to study completion. You will ensure informed consent processes comply with 45 CFR part 46 and maintain source records across multiple sites.

Join a team that adheres to FDA, ICH, and GCP guidelines, protects participant safety, and collaborates with investigators, sponsors, CROs, and IRBs. Prior nephrology experience is preferred.