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Part Time Clinical Research Jobs in Kansas (NOW HIRING)

IQVIA

Clinical Research Coordinator

Wichita, KS · On-site

$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 ...

Eye Care Partners

This includes specialists actively engaged in leading-edge research and equipped to handle the most ... dedicated to clinical excellence. Led by our Medical Executive Board, we are proud to offer ...

IQVIA

MedTech Field Service Tech Remediation

Wichita, KS · On-site

$30 - $32/hr

... clinical research services, commercial insights and healthcare intelligence to the life sciences ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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Part Time Clinical Research information

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

As of Aug 25, 2026, the average hourly pay for part time clinical research in Kansas is $20.26, according to ZipRecruiter salary data. Most workers in this role earn between $15.43 and $23.17 per hour, depending on experience, location, and employer.

What is a part-time clinical research position?

A part-time clinical research position involves assisting with the planning, implementation, and monitoring of clinical trials or studies on a reduced or flexible schedule, typically less than 40 hours per week. These roles may include tasks such as data collection, patient recruitment, regulatory documentation, and supporting principal investigators. Part-time clinical research jobs are common in hospitals, universities, and pharmaceutical companies, and they offer opportunities for students, healthcare professionals, or individuals seeking flexible work arrangements.

What are some common challenges faced in part-time clinical research roles, and how can they be managed?

Part-time clinical research professionals often encounter challenges balancing project deadlines with limited working hours, as studies may require timely data collection and reporting. Effective communication with the research team and proactive scheduling can help ensure tasks are completed efficiently. Additionally, staying organized and regularly updating project management tools can aid in tracking progress and maintaining compliance with protocols. Building strong relationships with full-time staff also supports seamless collaboration and knowledge sharing across shifts.

What are the key skills and qualifications needed to thrive as a part time clinical research professional, and why are they important?

To excel as a Part Time Clinical Research professional, you need a foundational understanding of clinical research methods, data collection, and regulatory guidelines, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification are typically required. Attention to detail, strong organizational skills, and effective communication help you manage multiple tasks and collaborate with research teams. These competencies ensure accurate data handling, regulatory compliance, and the smooth execution of research studies.

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

AspectPart Time Clinical ResearchPart Time Clinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldRequires a bachelor's degree; certification as a CRC is common
Work EnvironmentResearch sites, hospitals, clinics, or pharmaceutical companiesResearch sites, hospitals, clinics, often overseeing study activities
Employer & Industry UsageUsed across research organizations, biotech, pharmaPrimarily employed by research sites and clinical trial sponsors
Common Search & ComparisonOften compared for entry-level roles in clinical researchCompared for roles involving study coordination and participant management

Part Time Clinical Research roles focus on supporting clinical studies, often involving data collection and patient interactions. Part Time Clinical Research Coordinators have additional responsibilities in managing study protocols and participant coordination. Both roles require relevant education and certifications, but Coordinators typically have more oversight duties.

What are the most commonly searched types of Clinical Research jobs in Kansas?

The most popular types of Clinical Research jobs in Kansas are:

What are popular job titles related to Part Time Clinical Research jobs in Kansas?

For Part Time Clinical Research jobs in Kansas, the most frequently searched job titles are:

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

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

What cities in Kansas are hiring for Part Time Clinical Research jobs?

Cities in Kansas with the most Part Time Clinical Research job openings:

Part Time Clinical Research jobs near you
Infographic showing various Part Time Clinical Research job openings in Kansas as of August 2026, with employment types broken down into 2% As Needed, 75% Full Time, 16% Part Time, 1% Temporary, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $42,131 per year, or $20.3 per hour.

Clinical Research Coordinator

IQVIA

Wichita, KS • On-site

$35 - $42/hr

Part-time

Medical, Life

Re-posted 16 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 - 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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Benefits

Hours and flexibility

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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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