Onsite Clinical Research Coordinator

UroHealth Partners; Omaha (NE); On-site; USD 55,000 - 75,000; Full time

Job summary

UroHealth Partners is seeking a clinical research coordinator to support multiple studies onsite in Omaha, NE. You will work with the PI and team to coordinate enrollment, data collection, and study documentation, ensuring compliance with regulatory requirements.

The role requires healthcare credential (RN/LPN or Medical Assistant) and prior clinical research experience; strong organization, communication, and data management skills are essential.

Qualifications

• RN or LPN license or Medical Assistant certificate required.
• Two years in a clinical research setting preferred.
• Ability to coordinate visits, consent processes, and data collection.
• Strong attention to detail and knowledge of HIPAA.

Responsibilities

• Coordinates daily clinical trial activities and study conduct.
• Schedules participant visits and acts as patient liaison for PI and participating physicians.
• Reviews protocols, eligibility criteria, confidentiality, and privacy protections.
• Assists in informed consent process and explains study procedures to potential patients.
• Performs clinical procedures, data extraction from charts, and CRF completion.
• Coordinates sponsor visits and monitoring activities including audits.
• Maintains study regulatory binders and training materials.
• Ensures documentation and timely data submission for all study visits.
• Responds to data clarification requests and audit findings as needed.
• Obtains patient vitals and may perform phlebotomy.

Skills

Trial coordination

Patient recruitment

Informed consent

Regulatory compliance

Education

RN or LPN license

Medical Assistant certificate

Two years clinical research experience

Job description

UroHealth Partners is seeking a clinical research coordinator to support multiple studies onsite in Omaha, NE. You will work with the PI and team to coordinate enrollment, data collection, and study documentation, ensuring compliance with regulatory requirements.

The role requires healthcare credential (RN/LPN or Medical Assistant) and prior clinical research experience; strong organization, communication, and data management skills are essential.