Clinical Trails Coordinator
Monroe+Biomedical+Research•Monroe, NC
•Onsite
About The Position
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.
Requirements
- 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
Responsibilities
- 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
- 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
Benefits
- Growth Opportunity 🚀
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
