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Part Time H1B Clinical Research Jobs (NOW HIRING)

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 ...

IQVIA

Clinical Research Coordinator

Jefferson City, MO · On-site

$35 - $42/hr

Clinical Research Coordinator - Jefferson City, MO Work Set-Up: On-site Schedule Weekly Hours: 24 ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Research Coordinator

Cincinnati, OH · On-site

$35 - $42/hr

Clinical Research Coordinator - Cincinnati, OH Work Set-Up: On-site Schedule Weekly Hours: 24 hours ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Research Coordinator

Marietta, GA

$35 - $42/hr

Clinical Research Coordinator - Marietta, GA Work Set-Up: On-site Schedule Weekly Hours: 24 hours ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Main Line Health

Clinical Research Coord I

Wynnewood, PA

$23.25 - $31/hr

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... Clinical Research Coordinator I Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

Uofl

$23.25 - $31/hr

This is a part time temporary position scheduled to work 15 hours per week. Essential Duties and Responsibilities: * Facilitates compliance with the research protocol and Good Clinical Practice ...

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All JobsH1B Clinical Research JobsPart Time H1B Clinical Research Jobs

Part Time H1B Clinical Research information

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How much do part time h1b clinical research jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for part time h1b clinical research in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What are some common challenges faced by part time H1B clinical research professionals, and how can they be addressed?

Part-time H1B clinical research professionals often face challenges such as balancing visa compliance with limited working hours, integrating into research teams with full-time members, and managing complex regulatory requirements. To address these challenges, it's important to maintain clear communication with supervisors about work schedules, stay updated on visa regulations, and proactively seek opportunities for collaboration and professional development. Building strong relationships with colleagues and participating in team meetings, even remotely, can help ensure effective teamwork and integration.

What are the key skills and qualifications needed to thrive as a part time H1B clinical researcher?

To thrive as a Part Time H1B Clinical Researcher, you need a background in life sciences or healthcare, experience with research methodologies, and eligibility to work under H1B visa requirements. Familiarity with data analysis software, electronic data capture (EDC) systems, and regulatory compliance certifications such as GCP are typically required. Strong attention to detail, effective communication, and organizational skills are valuable soft skills in this role. These competencies ensure that research is conducted ethically, accurately, and efficiently, supporting high-quality scientific outcomes and regulatory compliance.

Are part time H1B clinical research jobs in demand?

Part-time H1B clinical research jobs are in demand due to ongoing clinical trials and the need for skilled research professionals. These roles often require knowledge of Good Clinical Practice (GCP) and familiarity with research tools, making them attractive for candidates seeking flexible schedules in the healthcare and research sectors.

What is the difference between Part Time H1B Clinical Research vs Part Time H1B Medical Assistant?

AspectPart Time H1B Clinical ResearchPart Time H1B Medical Assistant
Required CredentialsResearch-related certifications, bachelor's degree in health/scienceMedical assisting certification, high school diploma or equivalent
Work EnvironmentResearch labs, clinical trial sitesHospitals, clinics, outpatient facilities
Employer & IndustryPharmaceutical companies, research organizationsHospitals, outpatient clinics, healthcare providers
Common Search & ComparisonPart Time H1B Clinical Research vs Part Time H1B Medical Assistant

While both roles involve healthcare settings, Part Time H1B Clinical Research focuses on conducting clinical trials and research activities, requiring research-specific credentials. In contrast, Part Time H1B Medical Assistants support patient care directly in clinical environments, often needing medical assisting certifications. Understanding these differences helps international professionals choose the right career path aligned with their credentials and interests.

What is a part time H1B clinical research?

Part Time H1B Clinical Research jobs are roles in clinical research that are offered on a part-time basis to individuals holding or seeking an H1B visa in the United States. These positions typically involve assisting with medical studies, data collection, and patient care under the supervision of licensed professionals. H1B visa holders can work part-time if their employer files a petition specifying the part-time nature of the job, and the hours must comply with U.S. immigration regulations. These roles are ideal for those seeking research experience while managing other commitments or education.
More about Part Time H1B Clinical Research jobs
What cities are hiring for Part Time H1B Clinical Research jobs? Cities with the most Part Time H1B Clinical Research job openings:
What are the most commonly searched types of H1B Clinical Research jobs? The most popular types of H1B Clinical Research jobs are:
What states have the most Part Time H1B Clinical Research jobs? States with the most job openings for Part Time H1B Clinical Research jobs include:
What job categories do people searching Part Time H1B Clinical Research jobs look for? The top searched job categories for Part Time H1B Clinical Research jobs are:
Part Time H1B Clinical Research jobs near you
Infographic showing various Part Time H1B Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Coordinator

IQVIA

Raleigh, NC • Remote

$35 - $42/hr

Part-time

Medical, Life

Posted 14 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.

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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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