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Part Time Clinical Research Contract Jobs (NOW HIRING)

IQVIA

Clinical Research Coordinator

Wichita, KS

$35 - $42/hr

On-site Schedule: Part-time, 24 hours per week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare ...

Wisconsin

Clinical Research Coordinator

Madison, WI · On-site

$24.50 - $32.50/hr

This position is full or part-time, 90%-100% * This position may require some work to be performed ... A Clinical Research Coordinator II will perform tasks more independently, collect more complex ...

IQVIA

Clinical Research Coordinator

Albuquerque, NM

$35 - $42/hr

Onsite Schedule: 24 Hours/Week (Parttime) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with leading pharmaceutical ...

Eisenhower

Clinical Research Coordinator

Rancho Mirage, CA · On-site

$24.75 - $32.75/hr

Good Clinical Practice (GCP) Course, Clinical Research Coordinator Foundations Course, Clinical ... Contract Research Organization (CRO) sites and other department staff members.9. Manages the ...

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

Our commitment to excellence in clinical research operations ensures the highest standards of ... This is a part-time position that requires working one week per month on-site according to the ...

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

$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 ...

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Part Time Clinical Research Contract information

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

As of Aug 23, 2026, the average hourly pay for part time clinical research contract 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 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 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 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 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.

More about Part Time Clinical Research Contract jobs

What cities are hiring for Part Time Clinical Research Contract jobs?

Cities with the most Part Time Clinical Research Contract job openings:

What are the most commonly searched types of Part Time Clinical Research jobs?

The most popular types of Part Time Clinical Research jobs are:

What states have the most Part Time Clinical Research Contract jobs?

States with the most job openings for Part Time Clinical Research Contract jobs include:

What job categories do people searching Part Time Clinical Research Contract jobs look for?

The top searched job categories for Part Time Clinical Research Contract jobs are:

Part Time Clinical Research Contract jobs near you
Infographic showing various Part Time Clinical Research Contract job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Coordinator

IQVIA

Wichita, KS

$35 - $42/hr

Part-time

Medical, Life

Re-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

63rd of 225 rated it services

Job description

Clinical Research Coordinator - Wichita, KS
Work Set-Up: On-site
Schedule: Part-time, 24 hours per week

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. By combining deep scientific expertise with advanced technology, we deliver high-quality insights and support that help shape the future of clinical research.

About the Role

IQVIA is seeking a Clinical Research Coordinator (CRC) to support the successful execution of clinical research studies under the guidance of the Principal Investigator. This role is ideal for candidates with hands-on clinical research experience who are passionate about patient care, data quality, and advancing healthcare innovation.

The CRC will play a critical role in study coordination, patient engagement, clinical procedures, and data management while ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

Key Responsibilities

  • Perform clinical procedures including ECGs, vital signs, specimen/sample collection, and other protocol-required activities.

  • Coordinate and support daily clinical trial activities in compliance with study protocols, GCP, and site procedures.

  • Conduct patient chart reviews and prescreening activities to identify potentially eligible participants.

  • Recruit, screen, schedule, and orient study participants while ensuring patient safety and a positive participant experience.

  • Support patient visits and assist with study-related documentation and follow-up activities.

  • Prepare study materials, maintain study supplies, and assist with equipment setup and logistical planning.

  • Collect, review, and accurately document clinical data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems.

  • Support EDC data entry, query resolution, and data quality review in collaboration with investigators, sponsors, and monitors.

  • Respond to sponsor and monitor queries in a timely and accurate manner.

  • Maintain confidentiality, regulatory compliance, and adherence to Health & Safety policies.

  • Act as a patient advocate and contribute to a collaborative and professional research environment.

Qualifications

  • Bachelor's degree preferred, or an equivalent combination of education and relevant experience.

  • Minimum of 1+ years of relevant clinical research experience.

  • Working knowledge of clinical trials, GCP guidelines, and medical terminology.

  • Experience with patient chart review and prescreening activities.

  • Ability to support patient visits and study coordination activities in a clinical research environment.

  • Experience with EDC systems, including data entry and query resolution.

  • Strong attention to detail with excellent organizational and communication skills.

  • Ability to build effective working relationships with patients, investigators, sponsors, and team members.

Please Note

This position is not eligible for sponsorship.

#LI-CES #LI-DNP #LI-HCP #ONSITE

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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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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