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Part Time Clinical Research Contract Jobs in Raleigh, NC

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

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 ...

5PY IQVIA RDS Inc.

Research Associate

Durham, NC · On-site

$47K - $169K/yr

IQVIA is a leading global provider of clinical research services, commercial insights and health ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

5PY IQVIA RDS Inc.

Research Associate

Durham, NC

$47K - $169K/yr

IQVIA is a leading global provider of clinical research services, commercial insights and health ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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All JobsClinical Research Contract JobsPart Time Clinical Research Contract JobsPart Time Clinical Research Contract Jobs in Raleigh, NC

Part Time Clinical Research Contract information

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$11

$39

$67

How much do part time clinical research contract jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for part time clinical research contract in Raleigh, NC is $39.98, according to ZipRecruiter salary data. Most workers in this role earn between $28.03 and $51.15 per hour, depending on experience, location, and employer.

What is the difference between Part Time Clinical Research Contract vs Part Time Clinical Research Coordinator?

AspectPart Time Clinical Research ContractPart Time Clinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree in health sciences or related field; often holds certifications like CCRP or CRC
Work EnvironmentTemporary, project-based settings within research organizations or pharmaceutical companiesOngoing role within clinical sites or research organizations, overseeing study activities
Employer & Industry UsageUsed by research organizations, pharmaceutical companies, and CROs for specific projectsCommonly employed by hospitals, research centers, and clinical trial sites

In summary, a Part Time Clinical Research Contract is a temporary, project-specific role often filled by professionals with relevant certifications, while a Part Time Clinical Research Coordinator is a more ongoing position responsible for managing daily study activities at clinical sites. Both roles require similar credentials but differ in scope and employment type.

What are the typical responsibilities and challenges faced in a part time clinical research contract role?

In a part-time clinical research contract role, you may be responsible for tasks such as data collection, patient recruitment, regulatory documentation, and coordinating study visits, often within a limited number of hours each week. One common challenge is balancing multiple studies or priorities while adhering to strict compliance and reporting deadlines. You’ll frequently collaborate with research coordinators, principal investigators, and sometimes sponsors to ensure the smooth progress of clinical trials. Adapting quickly to evolving protocols and maintaining clear communication with the team are key to success in this flexible, yet demanding, position.

What is a part time clinical research contract?

A part-time clinical research contract is a work agreement where an individual is hired to assist with clinical research projects on a part-time basis, typically for a set duration or specific project. These contracts often involve roles such as study coordination, data collection, patient recruitment, or regulatory compliance. The part-time nature allows flexibility in hours and workload, making it ideal for students or professionals seeking supplementary experience. Contract terms, responsibilities, and compensation are usually outlined clearly before work begins. This arrangement benefits both employers needing temporary or specialized help and workers seeking flexible opportunities.

What are the key skills and qualifications needed to thrive as a part time clinical research contract professional?

To thrive in a Part Time Clinical Research Contract role, you need a solid understanding of clinical research processes, regulatory compliance, and relevant science or healthcare education. Familiarity with tools such as clinical trial management systems (CTMS), electronic data capture (EDC), and knowledge of GCP (Good Clinical Practice) guidelines or related certifications is often required. Strong organizational skills, attention to detail, and effective communication are critical soft skills for coordinating studies and liaising with stakeholders. These competencies ensure protocol adherence, data integrity, and successful collaboration within research teams.
What are the most commonly searched types of Part Time Clinical Research jobs in Raleigh, NC? The most popular types of Part Time Clinical Research jobs in Raleigh, NC are:
What are popular job titles related to Part Time Clinical Research Contract jobs in Raleigh, NC? For Part Time Clinical Research Contract jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Part Time Clinical Research Contract jobs in Raleigh, NC look for? The top searched job categories for Part Time Clinical Research Contract jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Part Time Clinical Research Contract jobs? Cities near Raleigh, NC with the most Part Time Clinical Research Contract job openings:
Part Time Clinical Research Contract jobs near you
Infographic showing various Part Time Clinical Research Contract job openings in Raleigh, NC as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $83,154 per year, or $40 per hour.

Clinical Research Coordinator

IQVIA

Raleigh, NC • Remote

$35 - $42/hr

Part-time

Medical, Life

Posted 12 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 223 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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