Clinical Trials Coordinator (RN/LPN/MA Background Preferred)

Louisville. KY (Onsite)

About the Role

At Monroe Biomedical Research, we are growing, and we're looking for a driven, patient-focused experienced Clinical Research Coordinator to join our team immediately.


This is a hands-on opportunity to be at the forefront of clinical trials, working directly with patients and contributing to research that advances medicine. If you thrive in a fast-paced environment, enjoy meaningful patient interaction, and take pride in precision and quality, this role is for you.


What You'll Do


Key Responsibilities

• Coordinate and execute clinical trial visits form screening through follow-up

• Maintain accurate source documentation in alignment with study protocols

• Perform clinical procedures such as phlebotomy, ECGs, and vital signs
• Ensure compliance with GCP, FDA, and sponsor requirements
• Educate and support participants throughout their study experience

Qualifications

• CMA, LPN, or RN strongly preferred
• Associate's degree required; Bachelor's preferred
• Experience in patient care, healthcare, or clinical research
• Strong attention to detail and organizational skills
• Ability to manage multiple studies in a fast-paced setting

Why Join Monroe Biomedical Research?

• Growing clinical research organization
• Collaborative, supportive team environment
• Opportunity to work on diverse clinical trials

Career Growth

High performers may advance into Lead CRC roles within 12-18 months.