Clinical Research Coordinator– Monroe, NC
We are seeking qualified, motivated, and detail-oriented Clinical Research Coordinators with a minimum of 2 years of clinical research experience to join our growing team in Monroe, NC.
The ideal candidate will have hands-on experience coordinating clinical trials, managing study participants, performing clinical assessments, maintaining accurate documentation, and ensuring compliance with study protocols and regulatory requirements.
WHAT YOU’LL DO:
Clinical Research & Study Management:
- Coordinate clinical trial visits from screening through study completion.
- Review study protocols and ensure all procedures are completed accurately and within required timelines.
- 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 Good Clinical Practice (GCP), FDA regulations, sponsor requirements, and internal procedures.
Patient Care & Clinical Responsibilities:
- Provide clinical support and care to adult study participants in accordance with study protocols, training, and applicable scope of practice.
- Perform clinical procedures as trained and qualified, including:
- Blood draws/phlebotomy
- ECGs
- Pulmonary function testing
- Vital signs
- Other protocol-required assessments
- Review medical histories, medications, laboratory results, and other clinical information.
- Educate participants on study procedures, medications, and follow-up requirements.
- Recognize and promptly communicate adverse events and clinically significant findings.
- Deliver a professional, compassionate, and patient-centered experience.
Data & Documentation
- Document study visits, clinical findings, and participant information accurately.
- Enter and maintain study data in sponsor systems within required timelines.
- Process and coordinate laboratory specimens according to study protocols.
- Respond to data queries and maintain accurate, complete, and inspection-ready study records.
QUALIFICATIONS:
- Minimum of 2 years of clinical research experience required.
- Previous experience as a Clinical Research Coordinator or in a similar clinical research role.
- Hands-on experience coordinating clinical trials and managing study participants.
- Experience with clinical assessments and procedures, including phlebotomy, ECGs, and vital signs, preferred.
- Working knowledge of GCP, FDA regulations, and clinical research requirements.
- Strong understanding of clinical trial protocols and study documentation.
- Excellent organizational skills and attention to detail.
- Ability to manage multiple priorities in a fast-paced environment.
- Strong communication and interpersonal skills.
- Professional, compassionate, and patient-focused approach.
- Must be able to commute daily to Monroe, NC.
WHY JOIN MONROE BIOMEDICAL RESEARCH?
- Join a growing clinical research organization.
- Be part of innovative clinical research and help advance medical treatments.
- Make a meaningful impact on participants and the future of medicine.
- Work alongside a collaborative, mission-driven team.
- Gain experience across a variety of clinical studies.
- Build opportunities for professional growth and career advancement.
Please apply only once. Thank you for your interest in joining Monroe Biomedical Research!