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Remote Clinical Research Protocol Writer Jobs in Raleigh, NC

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

  • Medical

  • Life

Coordinate and support clinical research studies in accordance with study protocols, sponsor ... This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

Conduct on-site and remote visits/contacts, including Qualification, Initiation, Monitoring ... Perform report review of visit reports of junior CRAs to ensure compliance with GCP and Protocol ...

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Senior Clinical Research Associate

Raleigh, NC · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

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Senior Clinical Research Associate

Cary, NC · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

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Senior Clinical Research Associate

Raleigh, NC · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

RemX

Be Seen First

Project Reconciliation Analyst - Clinical Research

Raleigh, NC · Remote

$60K - $72K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

NOW HIRING! Project Reconciliation Analyst Direct Hire | Remote | $60,000 - $72,000 Are you a ... Excellent written and verbal communication skills. * Ability to manage multiple priorities in a ...

New

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

... study designs, and protocol writing. Knowledge of applicable clinical research regulatory ... Maintaining a logical and organized approach to execution #LI-Remote #LI-NITINMAHAJAN IQVIA is a ...

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Remote Clinical Research Protocol Writer information

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How much do remote clinical research protocol writer jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for remote clinical research protocol writer in Raleigh, NC is $52.83, according to ZipRecruiter salary data. Most workers in this role earn between $38.80 and $62.40 per hour, depending on experience, location, and employer.

How does a remote clinical research protocol writer typically collaborate with research teams and stakeholders?

As a Remote Clinical Research Protocol Writer, you will frequently collaborate with cross-functional teams such as clinical trial managers, biostatisticians, regulatory affairs specialists, and medical experts. Communication often occurs through virtual meetings, emails, and shared document platforms to ensure all protocol elements meet regulatory, ethical, and scientific standards. You may be responsible for gathering input, incorporating feedback, and ensuring that protocols are clear and aligned with study objectives. This collaborative process is essential for creating robust documents that support successful study execution and regulatory submissions.

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

To excel as a Remote Clinical Research Protocol Writer, you need a background in life sciences or healthcare, strong scientific writing skills, and familiarity with regulatory guidelines such as GCP and ICH. Proficiency in tools like Microsoft Office, reference management software, and electronic data capture (EDC) systems is commonly required. Exceptional attention to detail, time management, and the ability to collaborate virtually with multidisciplinary teams are vital soft skills. These competencies ensure the creation of accurate, compliant, and clear research protocols that support successful clinical trials and regulatory submissions.

What does a remote clinical research protocol writer do?

A Remote Clinical Research Protocol Writer is responsible for creating detailed documents that outline the objectives, design, methodology, and organization of clinical research studies. They collaborate with clinical teams, researchers, and regulatory experts to ensure that protocols comply with regulatory standards and support the scientific goals of the study. Working remotely, they use digital tools to gather data, review literature, and communicate with stakeholders. Their work is essential for guiding clinical trials, ensuring participant safety, and supporting regulatory submissions.

What is the difference between Remote Clinical Research Protocol Writer vs Remote Clinical Research Associate?

AspectRemote Clinical Research Protocol WriterRemote Clinical Research Associate
CredentialsTypically requires a degree in life sciences, clinical research certification preferredRequires a degree in life sciences or related field, often with GCP or ICH certifications
Work EnvironmentPrimarily writing and editing protocols remotely, collaborating with teamsMonitoring clinical sites remotely, ensuring protocol compliance
Industry UsageUsed mainly in pharmaceutical and biotech companies for protocol developmentUsed across clinical trial sites for monitoring and data collection

The Remote Clinical Research Protocol Writer focuses on creating and editing clinical trial protocols, while the Remote Clinical Research Associate is responsible for monitoring trial sites and ensuring compliance. Both roles require knowledge of clinical research processes and often share similar certifications, but their daily tasks and work environments differ significantly.

What are the most commonly searched types of Clinical Research Protocol Writer jobs in Raleigh, NC?

The most popular types of Clinical Research Protocol Writer jobs in Raleigh, NC are:

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

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

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

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

What cities near Raleigh, NC are hiring for Remote Clinical Research Protocol Writer jobs?

Cities near Raleigh, NC with the most Remote Clinical Research Protocol Writer job openings:

Remote Clinical Research Protocol Writer jobs near you
Infographic showing various Remote Clinical Research Protocol Writer job openings in Raleigh, NC as of July 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $109,891 per year, or $52.8 per hour.

Clinical Research Coordinator

IQVIA

Raleigh, NC • Remote

$35 - $42/hr

Part-time

Medical, Life

Posted 20 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 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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Benefits

Hours and flexibility

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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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