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Remote Velocity Clinical Research Jobs in Raleigh, NC

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

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 ...

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

IQVIA

Director, Remote Research Clinicians

Durham, NC · Remote

Job Posting Title- Director, Remote Research Clinician/Decentralised Clinical Trials Location: Home ... Drive advancement of technology-enabled clinical trial solutions, including workflow automation ...

IQVIA

Director, Remote Research Clinicians

Durham, NC · Remote

Job Posting Title- Director, Remote Research Clinician/Decentralised Clinical Trials Location: Home ... Drive advancement of technology-enabled clinical trial solutions, including workflow automation ...

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 ...

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All JobsVelocity Clinical Research JobsRemote Velocity Clinical Research JobsRemote Velocity Clinical Research Jobs in Raleigh, NC

Remote Velocity Clinical Research information

See Raleigh, NC salary details

$10.7K

$77.2K

$133.7K

How much do remote velocity clinical research jobs pay per year?

As of Aug 25, 2026, the average yearly pay for remote velocity clinical research in Raleigh, NC is $77,219.00, according to ZipRecruiter salary data. Most workers in this role earn between $32,100.00 and $132,700.00 per year, depending on experience, location, and employer.

What is a remote Velocity Clinical Research job?

A Remote Velocity Clinical Research job involves conducting or supporting clinical trials and research activities from a remote location, often from home. The 'velocity' aspect typically refers to roles at Velocity Clinical Research, a company specializing in efficient, high-quality clinical trials. Employees in these positions may work as study coordinators, data managers, or administrative staff, helping to collect, manage, and analyze data for pharmaceutical or medical studies. Remote roles allow for flexibility while contributing to the advancement of medical science and patient care. Such positions generally require strong communication skills, attention to detail, and experience in clinical research processes.

How does working remotely in a Velocity Clinical Research role impact collaboration with site teams and study sponsors?

In a remote Velocity Clinical Research position, collaboration is primarily facilitated through digital platforms such as video conferencing, project management tools, and secure data systems. Team members may face the challenge of building rapport and maintaining clear communication with on-site staff and sponsors, but regular virtual meetings and well-defined procedures help bridge this gap. The remote environment supports flexibility and autonomy, while still emphasizing the importance of timely updates and proactive problem-solving to ensure study milestones are met. Successful collaboration often relies on strong organizational skills and a willingness to engage across time zones.

What are the key skills and qualifications needed to thrive as a remote Clinical Research Coordinator at Velocity Clinical Research, and why are they important?

To excel as a Remote Clinical Research Coordinator at Velocity Clinical Research, you typically need a background in life sciences or healthcare, experience in clinical trials, and familiarity with regulatory guidelines like GCP. Proficiency with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and remote communication tools is important. Strong organizational skills, attention to detail, and the ability to communicate effectively in virtual settings set top candidates apart. These skills ensure protocol compliance, data integrity, and smooth collaboration in a remote, regulated research environment.

What is the difference between Remote Velocity Clinical Research vs Remote Clinical Research Coordinator?

AspectRemote Velocity Clinical ResearchRemote Clinical Research Coordinator
CredentialsTypically requires life sciences or healthcare background, certifications like CCRP or RACRequires similar healthcare or research background, often with certifications like CCRP
Work EnvironmentRemote, office-based or home-based settings, collaborating with sponsors and sitesPrimarily remote, coordinating clinical trial activities across sites and vendors
Employer & Industry UsageContract research organizations, pharmaceutical companies, biotech firmsResearch sites, CROs, pharmaceutical companies

Remote Velocity Clinical Research and Remote Clinical Research Coordinator roles share similar credentials and work environments, both operating remotely within the clinical research industry. The main difference lies in their focus: Remote Velocity Clinical Research often involves managing multiple projects for CROs and sponsors, while Remote Clinical Research Coordinators typically handle site-level trial coordination. Both roles are essential in advancing clinical trials remotely, with overlapping skills and industry usage.

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

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

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

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

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

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

Remote Velocity Clinical Research jobs near you
Infographic showing various Remote Velocity Clinical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 13% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $77,219 per year, or $37.1 per hour.

Clinical Research Coordinator

IQVIA

Raleigh, NC • Remote

$35 - $42/hr

Part-time

Medical, Life

Posted 29 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 225 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

Pay

Benefits

Hours and flexibility

Workplace

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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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