Clinical Research Coordinator

Position Summary

The Clinical Research Coordinator (CRC) is responsible for the coordination, implementation, and management of clinical research studies conducted at Blue Ridge Associates in Neurology. The CRC supports clinical trials focused on Multiple Sclerosis, neuroimmunology, and related neurological conditions, ensuring that all research activities are conducted in accordance with study protocols, federal regulations, sponsor requirements, and institutional policies.

This position plays a critical role in advancing therapeutic innovation while ensuring patient safety, regulatory compliance, and data integrity.

Reporting Relationship:

Practice Manager

Responsibilities of the Clinical Research Coordinator include the following:

• Coordinate and manage all aspects of assigned clinical trials from study initiation through close-out
• Screen, recruit, and consent eligible study participants in accordance with protocol and regulatory guidelines
• Educate patients and families regarding study participation, procedures, risks, and benefits
• Schedule and conduct study visits in collaboration with investigators and clinical staff
• Collect, document, and maintain accurate study data and source documentation
• Ensure timely and accurate data entry into electronic data capture systems
• Monitor and report adverse events in accordance with sponsor and regulatory requirements
• Maintain regulatory binders and ensure compliance with FDA, GCP, HIPAA, and IRB standards
• Prepare for and participate in sponsor monitoring visits, audits, and inspections
• Coordinate study-related laboratory procedures, imaging, infusion therapy, and other protocol-specific services
• Communicate effectively with sponsors, contract research organizations (CROs), and internal clinical teams
• Assist with feasibility assessments and study start-up activities
• Support the administration of IV and infusion therapies, including patient monitoring and documentation, as needed.
  
  
  

Qualifications

• Bachelor’s degree in a health-related field or equivalent clinical research experience
• Minimum of 2–5 years of clinical research experience preferred
• Current, active Licensed Practical Nurse (LPN) license
• Experience in neurology, Multiple Sclerosis, autoimmune disorders, or infusion-based studies strongly preferred
• Knowledge of Good Clinical Practice (GCP), FDA regulations, and IRB processes
• Strong organizational, documentation, and time management skills
• Ability to manage multiple studies simultaneously
• Proficiency with electronic medical records and clinical trial management systems
  
  
  

Certification as a Clinical Research Coordinator (CCRC or CCRP) is preferred but not required.

Work Environment

This position operates primarily in a clinical and research office environment within the Salem and Christiansburg locations. Direct patient interaction and on-site presence are required.

Physical Requirements

The physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions in this job description:

• The employee is regularly required to stand, walk, and sit, as well as talk and hear.
• Good hand-eye coordination and the ability to lift up to at least 25 pounds.