Job detail

Clinical Trails Coordinator

Monroe+Biomedical+Research

#CMA #RN #Medical Records #FDA #Phlebotomy #Healthcare #Lab Specimens #Clinical Research #GCP #Clinical Trials

Quick overview

Manage clinical trial patient visits and maintain accurate source documentation in compliance with GCP and FDA requirements. Perform clinical procedures such as blood draws and ECGs while managing study data in sponsor systems.

Requirements summary

Requires an associate's degree, with a bachelor's degree and CMA or RN certification strongly preferred. Candidates must have prior experience in healthcare or clinical research and proficiency in performing clinical procedures.

associate degreebachelor degreeprofessional certificateAttention To DetailInterpersonal CommunicationPatient CarePhlebotomyPatient EducationData EntryVital SignsSource DocumentationMedical Record ReviewClinical Research CoordinationFDA RegulationsECGStudy ManagementGCP CompliancePulmonary Function TestsLab Specimen Handling

Job description

Clinical Research Coordinator 📍 Monroe Biomedical Research- Monroe, NC 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 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 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.

Clinical Trails Coordinator

Quick overview

Requirements summary

Job description

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