Clinical Trials Coordinator - Monroe- NC
Urgent Need for experience CRCs
📍 Monroe Biomedical Research- Monroe, NC
At Monroe Biomedical Research, we are growing, and we’re looking for a driven, patient-focused experienced Clinical Trials 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
Study Management
- Develop and maintain accurate source 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
- Data & Documentation
- 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
What We’re Looking For
- Certified Medical Assistant (CMA) or Registered Nurse (RN) strongly preferred
- Associate’s degree required; Bachelor’s degree preferred
- Prior experience in healthcare, clinical research, or direct patient care
- Experience performing clinical procedures (phlebotomy, vitals, ECGs, etc.)
- Strong attention to detail with the ability to manage multiple priorities
- Excellent communication and interpersonal skills
- A proactive, team-oriented mindset with a commitment to patient-centered care
- Must commute to Monroe, NC. This is an onsite position.
Why Join Monroe Biomedical Research?
- Be part of a rapidly growing clinical research organization
- Make a direct impact on cutting-edge medical advancements
- Work alongside a collaborative, mission-driven team
- Gain hands-on experience across a variety of clinical studies
Growth Opportunity 🚀
We invest in our people. This role offers a clear path to advancement into a Lead Clinical Research Coordinator position within 12–18 months based on performance.
Skills Required
- Associate's degree
- Certified Medical Assistant (CMA) or Registered Nurse (RN)
- Bachelor's degree
- Prior experience in healthcare, clinical research, or direct patient care
- Experience performing clinical procedures (phlebotomy, ECGs, pulmonary function tests, vitals)
- Knowledge of GCP, FDA, and sponsor requirements / regulatory compliance
- Ability to develop and maintain accurate source documentation and manage multiple priorities
- Experience with data entry and managing study data in sponsor systems
- Excellent communication and interpersonal skills; patient-focused mindset
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.
