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Remote Clinical Research Coverage Analyst Jobs in Raleigh, NC

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

... analytics, technology solutions, and clinical research services, dedicated to driving healthcare ... This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA ...

RemX

Be Seen First

Project Reconciliation Analyst - Clinical Research

Raleigh, NC · Remote

$60K - $70K/yr

Project Reconciliation Analyst Direct Hire | Remote | $60,000 - $70,000 Are you a detail-oriented finance professional with experience in the clinical research industry? We are seeking a Project ...

Labcorp

Sr. Clinical Research Associate

Durham, NC · On-site +1

Conduct remote monitoring activities appropriate for observational studies, including review of ... Collaborate with data management and analytics teams to support data quality review, query ...

IQVIA

Director, Remote Research Clinicians

Durham, NC · Remote

Drive advancement of technology-enabled clinical trial solutions, including workflow automation ... Support investigations, root cause analyses, and Corrective and Preventive Action (CAPA) activities.

IQVIA

Director, Remote Research Clinicians

Durham, NC · Remote

Drive advancement of technology-enabled clinical trial solutions, including workflow automation ... Support investigations, root cause analyses, and Corrective and Preventive Action (CAPA) activities.

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Clinical Research Associate II

Raleigh, NC · Remote

Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ... Life assurance and disability coverage * Employee assistance programmes and wellbeing resources

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Clinical Research Associate II

Cary, NC · Remote

Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ... Life assurance and disability coverage * Employee assistance programmes and wellbeing resources

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Clinical Research Associate II

Raleigh, NC · Remote

Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ... Life assurance and disability coverage * Employee assistance programmes and wellbeing resources

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All JobsClinical Research Coverage Analyst JobsRemote Clinical Research Coverage Analyst JobsRemote Clinical Research Coverage Analyst Jobs in Raleigh, NC

Remote Clinical Research Coverage Analyst information

See Raleigh, NC salary details

$37.4K

$71.9K

$96.7K

How much do remote clinical research coverage analyst jobs pay per year?

As of Sep 6, 2026, the average yearly pay for remote clinical research coverage analyst in Raleigh, NC is $71,900.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,400.00 and $95,800.00 per year, depending on experience, location, and employer.

What is a remote clinical research coverage analyst?

Remote Clinical Research Coverage Analysts are professionals who evaluate clinical research studies to determine which procedures and services are billable to insurance, sponsors, or research grants, all while working remotely. They review study protocols, informed consent documents, and payer policies to ensure compliance with regulations and institutional guidelines. Their work is critical in helping research organizations and hospitals avoid billing errors and maintain financial integrity for clinical trials. By working remotely, they leverage digital tools and secure systems to access and analyze study documents from any location.

What are the key skills and qualifications needed to thrive as a remote clinical research coverage analyst?

To thrive as a Remote Clinical Research Coverage Analyst, you need a solid understanding of clinical research billing, healthcare compliance regulations, and medical terminology, often supported by a bachelor’s degree in a health-related field. Familiarity with billing systems, electronic medical records (EMRs), Medicare Coverage Analysis (MCA) tools, and relevant certifications such as CCRC or ACRP are commonly required. Attention to detail, analytical thinking, and strong written communication help ensure accuracy and effective collaboration with remote teams. These skills and qualifications are crucial for ensuring regulatory compliance, minimizing financial risk, and supporting successful clinical trial operations.

How does a remote clinical research coverage analyst collaborate with clinical trial teams and ensure accurate coverage analysis from a distance?

As a Remote Clinical Research Coverage Analyst, you will frequently interact with study coordinators, investigators, billing teams, and compliance officers via virtual meetings, emails, and shared project management systems. Even though you work remotely, you are expected to review clinical trial protocols, determine qualifying status, and analyze billing grids to ensure that all patient care costs are accurately classified as either standard of care or research-related. Clear communication and strong organizational skills are essential to coordinate effectively, resolve discrepancies, and keep all stakeholders informed about regulatory and payer requirements. Regular updates and virtual check-ins with site teams help maintain alignment and ensure ongoing compliance.

What is the difference between Remote Clinical Research Coverage Analyst vs Remote Clinical Trial Coordinator?

AspectRemote Clinical Research Coverage AnalystRemote Clinical Trial Coordinator
Required CredentialsTypically requires a background in healthcare, clinical research certifications, and knowledge of coverage policiesRequires clinical trial management experience, good organizational skills, and often a degree in health sciences or related fields
Work EnvironmentPrimarily remote, focusing on coverage analysis, documentation, and complianceRemote or hybrid, coordinating trial activities, patient recruitment, and site communication
Employer & Industry UsagePharmaceutical companies, insurance providers, CROsResearch institutions, pharmaceutical companies, CROs

The Remote Clinical Research Coverage Analyst primarily focuses on evaluating insurance coverage and reimbursement policies for clinical trials, ensuring compliance and proper billing. In contrast, the Remote Clinical Trial Coordinator manages trial logistics, patient coordination, and site communication. Both roles are essential in clinical research but differ in their core responsibilities and skill sets.

What are popular job titles related to Remote Clinical Research Coverage Analyst jobs in Raleigh, NC?

For Remote Clinical Research Coverage Analyst jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Research Coverage Analyst jobs in Raleigh, NC look for?

The top searched job categories for Remote Clinical Research Coverage Analyst jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Remote Clinical Research Coverage Analyst jobs?

Cities near Raleigh, NC with the most Remote Clinical Research Coverage Analyst job openings:

Remote Clinical Research Coverage Analyst jobs near you
Infographic showing various Remote Clinical Research Coverage Analyst job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $71,900 per year, or $34.6 per hour.

Clinical Research Coordinator

IQVIA

Raleigh, NC • Remote

$35 - $42/hr

Part-time

Medical, Life

This job post has expired 2 days ago. Applications are no longer accepted.

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services

Job description

Clinical Research Coordinator (CRC) - Raleigh, NC

Location: Raleigh, NC
Work Setup: On-site
Schedule: 24 hours per week (Part-Time)

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world's leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. By combining deep scientific expertise with advanced technology, we help transform clinical research and bring new therapies to patients faster.

About the Role

IQVIA is seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to support the successful execution of clinical research studies under the direction of the Principal Investigator. This role offers the opportunity to work directly with research participants, contribute to groundbreaking clinical trials, and ensure the highest standards of patient care, data quality, and regulatory compliance.

The ideal candidate has hands-on clinical research experience, is comfortable performing study-related procedures, and possesses strong organizational skills in both data management and regulatory documentation.

Key Responsibilities

  • Coordinate and support clinical research studies in accordance with study protocols, sponsor requirements, and Good Clinical Practice (GCP) guidelines.

  • Perform study-related clinical procedures, including ECGs, vital signs, specimen collection, and other protocol-required assessments.

  • Recruit, screen, enroll, and educate study participants while ensuring participant safety and retention.

  • Prepare study materials, maintain equipment, and coordinate study logistics to support efficient study conduct.

  • Accurately collect, review, and enter study data into Electronic Data Capture (EDC) systems.

  • Review source documentation and ensure timely resolution of data queries and discrepancies.

  • Support regulatory activities, including maintaining electronic study files and ensuring documentation is audit-ready.

  • Collaborate with investigators, sponsors, monitors, and study team members to ensure protocol compliance and data integrity.

  • Serve as a patient advocate while maintaining a safe and compliant research environment.

Qualifications

Required

  • Minimum of 1 year of clinical research experience in a Clinical Research Coordinator or related role.

  • Working knowledge of clinical trial processes, GCP guidelines, and medical terminology.

  • Experience performing accurate clinical data entry and managing study documentation.

  • Familiarity with Electronic Data Capture (EDC) systems and data query resolution.

  • Strong organizational skills, attention to detail, and ability to manage multiple priorities in a fast-paced research environment.

  • Ability to build effective relationships with patients, investigators, sponsors, and study team members.

Preferred

  • Bachelor's degree in a health science, life science, or related field, or an equivalent combination of education and relevant experience.

  • Experience utilizing CRIO (Clinical Research IO) to review and receive source data prior to EDC entry.

  • Experience supporting regulatory processes, including electronic regulatory filing, document maintenance, and ensuring study documentation complies with sponsor and regulatory requirements.

  • Experience with source document review, data reconciliation, and maintaining high standards of data quality and compliance.

Please note: This position is not eligible for employment sponsorship.

#LI-CES and #LI-DNP #LI-HCP #remote

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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