Clinical Research Coordinator

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!