Louisville. KY (Onsite)
About the Role
AtMonroe Biomedical Research, we aregrowing,andwe'relooking for adriven, patient-focused experienced Clinical Research Coordinatorto join our teamimmediately.
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 andquality,this role is for you.
WhatYou'llDo
Study Management
- Develop andmaintainaccuratesource documentation aligned with study protocols
- Coordinate and manage clinical trial patient visits from start to finish
- Ensure studies are conducted in compliance with GCP, FDA, and sponsor requirements
- Patient Care & Interaction
- Perform clinical procedures including blood draws, ECGs, pulmonary function tests, and vital signs
- Provide a high-quality, supportive experience for study participants
- Educate and guide patients throughout their clinical trial journey
- Accurately review and process medical records
- Prepare, handle, and ship lab specimens per protocol guidelines
- Enter and manage study data in sponsor systems with precision and timeliness
Qualifications
- NP who can practice in an Adult population
- Masters Degree Required
- 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.