Clinical Research Coordinator

About The Role

Monroe Biomedical Research is seeking an experienced, patient-focused onsite Clinical Research Coordinator preferably with their (RN/NP) to join our Monroe, NC location. This hands-on role combines direct patient care with clinical research coordination.

What You’ll Do

• Clinical Research & Study Management
  • Coordinate clinical trial visits from screening through completion.
  • Review protocols and ensure study procedures are completed accurately and on schedule.
  • Maintain complete and accurate source documentation.
  • Support participant screening, enrollment, and ongoing study activities.
  • Collaborate with investigators, sponsors, monitors, and research staff.
  • Ensure compliance with GCP, FDA regulations, sponsor requirements, and internal procedures.
• Patient Care & Clinical Responsibilities
  • Provide clinical assessment and care to adult study participants within your scope of practice and study requirements.
  • Perform and/or oversee procedures including: Blood draws/phlebotomy, ECGs, Pulmonary function testing, Vital signs, Other protocol-required assessments.
  • Review medical history, medications, laboratory results, and other clinical information.
  • Educate participants on study procedures, medications, and follow-up.
  • Navigate and communicate adverse events or clinically significant findings.
  • Deliver a professional, compassionate, and patient-centered experience.
• Data & Documentation
  • Document study visits, clinical findings, and patient information accurately.
  • Enter and maintain study data within sponsor systems and required timelines.
  • Process and coordinate laboratory specimens according to protocol.
  • Respond to data queries and maintain accurate, inspection-ready records.

Qualifications

• Current RN or NP license with the ability to practice with an adult patient population.
• Bachelor’s degree in nursing required; Master’s degree for NP candidates.
• Previous direct patient care experience required.
• Clinical research experience is highly preferred.
• Strong clinical judgment and commitment to patient safety.
• Excellent organization, documentation, and attention to detail.
• Ability to interpret and follow detailed clinical trial protocols.
• Ability to manage multiple priorities in a fast-paced environment.
• Strong communication and interpersonal skills.
• Professional, compassionate, and patient-focused approach.
• Must commute daily to Monroe, NC daily.