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Part Time Medical Device Clinical Research Jobs in Raleigh, NC

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

We partner with the world's leading pharmaceutical, biotechnology, and medical device organizations ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Duke University

Clinical Research Intern

Durham, NC · On-site

$20 - $27.02/hr

Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive ... CLINICAL RESEARCH INTERN - Dr. Anthony Catanzano Jr. Lab Be You. This internship was created to ...

Duke University

Clinical Research Intern

Durham, NC · On-site

$20 - $27.02/hr

Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive ... CLINICAL RESEARCH INTERN - Dr. Anthony Catanzano Jr. Lab Be You. This internship was created to ...

NCSU

Research Technician

Raleigh, NC · On-site

$17.50 - $24/hr

Our world-leading faculty and clinicians are at the forefront of interdisciplinary biomedical ... Medical , Dental , and Vision * Flexible Spending Account * Retirement Programs * Disability Plans

NCSU

Research Scholar

Raleigh, NC

... and device/system design. We are now seeking to enhance and grow this effort in the areas of ... Medical, Dental, and Vision * Flexible Spending Account * Retirement Programs * Disability Plans

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All JobsMedical Device Clinical Research JobsPart Time Medical Device Clinical Research JobsPart Time Medical Device Clinical Research Jobs in Raleigh, NC

Part Time Medical Device Clinical Research information

See Raleigh, NC salary details

$47.6K

$104.3K

$183.7K

How much do part time medical device clinical research jobs pay per year?

As of Aug 16, 2026, the average yearly pay for part time medical device clinical research in Raleigh, NC is $104,339.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,700.00 and $119,100.00 per year, depending on experience, location, and employer.

What is the difference between Part Time Medical Device Clinical Research vs Part Time Medical Device Quality Assurance?

AspectPart Time Medical Device Clinical ResearchPart Time Medical Device Quality Assurance
Required CredentialsTypically requires a background in life sciences, clinical research certifications, or related degreesOften requires quality assurance certifications, such as ISO standards or GMP training
Work EnvironmentConducts studies in clinical settings, hospitals, or research facilitiesWorks in manufacturing sites, labs, or compliance departments
Employer & Industry UsageUsed by clinical research organizations, medical device companies, and hospitalsUsed by manufacturing firms, regulatory agencies, and quality departments

Part Time Medical Device Clinical Research focuses on conducting clinical trials and gathering data on medical devices, while Part Time Medical Device Quality Assurance ensures products meet safety and quality standards. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

What skills and qualifications are needed for a part time medical device clinical research professional?

To thrive in Part Time Medical Device Clinical Research, you need a background in life sciences or healthcare, knowledge of clinical trial protocols, and familiarity with regulatory requirements such as Good Clinical Practice (GCP). Experience with electronic data capture (EDC) systems, clinical trial management software, and possibly certifications like SOCRA or ACRP are highly beneficial. Strong attention to detail, communication skills, and the ability to work both independently and collaboratively make candidates stand out. These competencies are crucial for ensuring compliant, accurate, and efficient clinical research that supports medical device safety and efficacy.

What are the typical responsibilities of a part time medical device clinical research professional?

In a part-time medical device clinical research role, you will typically assist with study coordination, data collection, and documentation to ensure compliance with regulatory standards. This may involve supporting patient enrollment, monitoring trial progress, and helping to prepare reports or presentations. You will often collaborate closely with clinical research coordinators, investigators, and regulatory teams to ensure the study runs smoothly. The part-time nature of the job can offer flexibility, but it also requires excellent time management to balance multiple tasks and deadlines within limited hours.

What is a part time medical device clinical research?

A part time medical device clinical research job involves supporting clinical trials or studies that evaluate the safety and effectiveness of medical devices, but on a reduced or flexible schedule. Professionals in this role may assist with tasks such as data collection, patient monitoring, regulatory documentation, and coordinating with healthcare teams. These positions are ideal for those seeking work-life balance or who have other commitments, while still contributing to important medical advancements. Part time roles can be found in hospitals, research organizations, or medical device companies.

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

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

What are popular job titles related to Part Time Medical Device Clinical Research jobs in Raleigh, NC?

For Part Time Medical Device Clinical Research jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Part Time Medical Device Clinical Research jobs in Raleigh, NC look for?

The top searched job categories for Part Time Medical Device Clinical Research jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Part Time Medical Device Clinical Research jobs?

Cities near Raleigh, NC with the most Part Time Medical Device Clinical Research job openings:

Part Time Medical Device Clinical Research jobs near you
Infographic showing various Part Time Medical Device Clinical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 18% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $104,339 per year, or $50.2 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

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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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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