Clinical Research Coordinator
MONROE BIOMEDICAL RESEARCH LLC
Summary
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.
Job description
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.
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, and 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.
Requirements
- 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
Company overview
Monroe Biomedical Research LLC is a dedicated clinical research facility located in Monroe, North Carolina, near Charlotte. Founded in 2016, the company operates a 6,300 square foot research center that specializes in conducting clinical trials across various therapeutic areas. As a Contract Research Organization (CRO), Monroe Biomedical Research has established itself as one of the highest enrolling research centers in the nation with a proven Good Clinical Practice (GCP) record and a highly experienced study team. The company focuses on pharmaceutical testing and clinical research across multiple disease areas including COVID-19 vaccine testing, asthma, COPD, diabetes, heart failure, and hypertension clinical trials. Their expertise extends to clinical trial recruitment and treatment studies, serving pharmaceutical sponsors and biotech companies. With a team of 11-50 employees, Monroe Biomedical Research maintains strong industry connections and participates in major clinical research conferences like SCOPE Summit, demonstrating their commitment to advancing biomedical research and improving patient outcomes through rigorous clinical trial execution.