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

Posted 2 Days Ago
Be an Early Applicant
Louisville, KY, USA
In-Office
Entry level
Healthtech • Professional Services • Biotech • Pharmaceutical
The Role
Coordinate and execute clinical trial visits from screening through follow-up, perform clinical procedures (phlebotomy, ECGs, vitals), maintain accurate source documentation, ensure GCP/FDA/sponsor compliance, and educate/support study participants while managing multiple studies.
Summary Generated by Built In

📍 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.

Skills Required

  • CMA, LPN, or RN
  • Associate's degree
  • Bachelor's degree
  • Experience in patient care, healthcare, or clinical research
  • Perform clinical procedures (phlebotomy, ECGs, vital signs)
  • Knowledge of GCP, FDA, and sponsor requirements
  • Maintain accurate source documentation in alignment with study protocols
  • Strong attention to detail and organizational skills
  • Ability to manage multiple studies in a fast-paced setting
  • Participant education and support throughout study experience
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The Company
58 Employees

What We Do

Monroe Biomedical Research (MBR) is a multi-specialty clinical research organization operating fully owned research sites. The company specializes in conducting Phase 1-4 clinical trials across various therapeutic areas, including cardiometabolic, endocrinology, respiratory, and general medicine research for drugs, medical devices, and diagnostics. MBR partners with sponsors and CROs to deliver high-quality trial execution and a supportive, respectful experience for all research participants.

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