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

📍 Louisville (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.