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Clinical Research Coordinator

Blue Ridge Associates in Neurology
Remote

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Job Details

Qualifications

Full Job Description

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:

Director of Operations

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 remote setting; however, occasional travel to our clinics may be required. Candidates need to be based in Northeast Tennessee/Southwest Virginia region.

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.

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