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Clinical Research Associate Remote Jobs in Virginia

AbbVie

Clinical Research Associate II

Richmond, VA · On-site +1

$78K/yr

Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience.

Virginia Tech

Postdoctoral Associate

Blacksburg, VA · On-site +1

Postdoctoral Associate Apply now Back to search results Job no: 536160 Work type: Research Faculty ... Research / Scientific The postdoctoral researcher will work at the Hydrologic Innovation and Remote ...

HR Knowledge Source

Board Liaison (Remote)

Alexandria, VA · Remote

$85K - $90K/yr

To ensure that clinical research findings benefit all populations, NMF works to increase the number ... Remote, but must be able to work within the Eastern Time Zones to ensure adequate daily overlap ...

IQVIA

Senior Data Team Lead (Remote)

Richmond, VA · Remote

$86K - $217K/yr

Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

IQVIA

Senior Data Team Lead (Remote)

Virginia Beach, VA · Remote

$86K - $217K/yr

Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

IQVIA

Senior Data Team Lead (Remote)

Norfolk, VA · Remote

$86K - $217K/yr

Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

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Clinical Research Associate Remote information

What does a Clinical Research Associate do when working remotely?

A Clinical Research Associate (CRA) working remotely is responsible for monitoring clinical trials to ensure they comply with regulatory requirements and study protocols. They coordinate with clinical sites, review data, ensure proper documentation, and communicate findings with research teams—all from a remote location. While they may occasionally travel for on-site visits, most of their tasks, such as reviewing electronic records, participating in virtual meetings, and managing trial documentation, are performed online. Remote CRAs play a vital role in maintaining the integrity and quality of clinical studies.

What are some common challenges faced by Clinical Research Associates working remotely, and how can they be addressed?

Remote Clinical Research Associates often face challenges such as coordinating across different time zones, maintaining clear communication with site staff, and ensuring data integrity without being physically present. These challenges can be addressed by leveraging robust digital tools for project management and communication, setting clear expectations with research sites, and establishing regular virtual check-ins. Staying organized, proactive, and responsive is key to successfully managing multiple studies and fostering effective collaboration from a remote environment.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate (Remote), and why are they important?

To excel as a Clinical Research Associate (Remote), you generally need a background in life sciences or a related field, experience with clinical trial processes, and knowledge of regulatory guidelines like GCP. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and relevant certifications such as ACRP or SOCRA are highly valuable. Strong organizational, communication, and problem-solving skills are essential for managing remote monitoring and collaborating with research teams. These competencies ensure data integrity, regulatory compliance, and effective coordination across geographically dispersed clinical trial sites.
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Clinical Research Associate Remote jobs near you
Infographic showing various Clinical Research Associate Remote job openings in Virginia as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.

Clinical Research Coordinator

Blue Ridge Associates in Neurology

Christiansburg, VA • Remote

$20 - $22/hr

Full-time

Re-posted 12 days ago

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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