Clinical Research Coordinator

Job Description

Job Description

Salary : About the Role

Monroe Biomedical Research is preparing for a significant expansion of its clinical research operations, including new infrastructure and additional clinical trial site locations. We are seeking an ambitious Clinical Research Coordinator (CRC) to join our team and support this exciting growth phase.

As a CRC, you will be responsible for coordinating and executing clinical research activities on-site in Charleston, SC. You will interact directly with patients and internal staff, perform study procedures, and ensure accurate data collection and management. This role requires a meticulous, organized, and self-driven individual who is comfortable working independently and taking full ownership of their assigned clinical trials.

Key Responsibilities

• Design and maintain source documentation and workflows based on protocol requirements
• Organize and manage study patient visits
• Perform study procedures and collect clinical data (e.g., blood draws, ECGs, vital signs, spirometry)
• Review and process medical records
• Process and package laboratory specimens
• Communicate with, schedule, and provide guidance to study participants
• Submit and manage study data to pharmaceutical sponsors

Qualifications

What We Offer

Additional Information