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Monroe+Biomedical+Research logo

Clinical Trails Coordinator

Monroe+Biomedical+Research·Louisville, Kentucky

Full Time·On Site·2-5 yrs·Posted 1 day ago
Practice for this role

About the role

Coordinate and execute clinical trial visits from screening through follow-up while maintaining accurate source documentation. Perform clinical procedures including phlebotomy and ECGs while ensuring compliance with GCP and FDA requirements.

📍 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.

Requirements

An associate's degree is required, with a bachelor's degree and certifications such as CMA, LPN, or RN strongly preferred. Candidates should have experience in patient care or clinical research and the ability to manage multiple studies in a fast-paced environment.

  • associate degree
  • bachelor degree
  • Organizational Skills
  • Patient Care
  • Phlebotomy
  • Patient Education
  • Vital Signs
  • Source Documentation
  • FDA Regulations
  • ECG
  • GCP Compliance
  • Clinical Trial Coordination

Benefits

  • Career Growth Opportunities
  • Collaborative Team Environment

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
2-5 yrs
Location
Louisville, Kentucky
Posted
Jul 27, 2026
Application
Employer website
Monroe+Biomedical+Research logo

Hiring organization

Monroe+Biomedical+Research

Monroe Biomedical Research (MBR) is a multi-specialty clinical research organization operating fully owned research sites. MBR excels in Phase 1-4 cardiometabolic, endocrinology, and respiratory clinical trials, as well as general medicine studies for drugs, medical devices, and...

IndustryBiotechnology Research
TypePrivately Held
Size51-200 employees
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Market context

Kentucky LPN roles remain steady

Kentucky nursing employers commonly look for licensed practical nurses who can step into school, pediatric, or long-term care settings and handle routine care with confidence. These roles can be competitive because an active Kentucky LPN license, current CPR/BLS, and comfort with complex medical needs are often expected, while the benefits package may include paid holidays, personal time, sick time, and a 401(k) match. Review the AI-summarized requirements and benefits here to save research time, and confirm your license and certification status before applying.

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