What are the responsibilities and job description for the Clinical Research Coordinator position at Monroe+Biomedical+Research?
Monroe Biomedical Research (MBR) is expanding its clinical research operations, including new trial site locations and enhanced infrastructure. We are seeking a dedicated and detail-oriented Clinical Research Coordinator (CRC) to join our team and play a critical role in advancing clinical research.
Why Join Us? Growing Organization: Be part of an expanding research facility with opportunities for career advancement.
Impactful Work: Help drive medical advancements by working directly with patients and healthcare professionals.
Support & Training: Receive hands-on training while working independently to manage clinical trials.
- Coordinate and oversee clinical trial activities, ensuring compliance with study protocols.
- Design and maintain source documentation and workflows.
- Schedule and conduct study visits with patients.
- Perform study procedures, including:
- Blood draws, ECGs, breathing tests, and vital sign measurements.
- Process and submit medical records, study data, and laboratory samples.
- Communicate with patients, ensuring high-quality care and compliance.
- Education: Associates degree or relevant experience required; Bachelors degree preferred.
- Experience: Prior experience in healthcare, clinical research, or as a medical assistant (LPN, CRC, etc.) preferred.
- Skills: Strong multitasking abilities, attention to detail, and excellent interpersonal skills.
- Ambition: Desire to grow into a lead coordinator role within 12-18 months.
Competitive salary
Matching 401(k)
Performance-based bonuses
Company-paid Health, Dental, & Vision Insurance*
Career growth in a fast-expanding research organization
Convenient Monroe location with easy highway access to Charlotte
Important: This is a 100% onsite role. Only candidates local to Monroe or the Charlotte, NC area will be considered.
Apply today and become part of a team making a real difference in clinical research!
