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Part Time Clinical Data Manager Jobs in Kansas (NOW HIRING)

IQVIA

Clinical Research Coordinator

Wichita, KS · On-site

$35 - $42/hr

... procedures, and data management while ensuring compliance with study protocols, regulatory ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Pawnee Mental Health

Crisis Clinical Manager

Manhattan, KS · On-site

$100K/yr

... part time benefits specialist work. Focus is on housing and connection to appropriate benefits to ... data requirements for grant programs and other state reporting needs. · Review client incidents ...

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All JobsClinical Data JobsPart Time Clinical Data Manager JobsPart Time Clinical Data Manager Jobs in Kansas

Part Time Clinical Data Manager information

See Kansas salary details

$44.2K

$98.1K

$145.5K

How much do part time clinical data manager jobs pay per year?

As of Aug 1, 2026, the average yearly pay for part time clinical data manager in Kansas is $98,127.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,400.00 and $116,500.00 per year, depending on experience, location, and employer.

What does a Part Time Clinical Data Manager do?

A Part Time Clinical Data Manager is responsible for collecting, managing, and ensuring the accuracy of data generated from clinical trials, but on a reduced or flexible schedule. Their duties include designing data collection systems, monitoring data quality, ensuring compliance with regulatory standards, and collaborating with clinical research teams. Working part-time allows them to handle these responsibilities while maintaining a balanced workload, often supporting multiple studies or phases as needed. They play a crucial role in ensuring that clinical trial data is reliable and ready for statistical analysis and regulatory submission.

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

AspectPart Time Clinical Data ManagerPart Time Clinical Research Coordinator
CredentialsTypically requires a degree in health sciences, life sciences, or related field; certifications like CDMP are commonRequires a degree in health sciences or related field; certifications are less common but may include CRC certification
Work EnvironmentWorks primarily with data management systems, databases, and electronic records in clinical trial settingsManages study logistics, patient interactions, and site coordination in clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch institutions, hospitals, clinical trial sites

While both roles support clinical trials, the Part Time Clinical Data Manager focuses on data accuracy and database management, whereas the Part Time Clinical Research Coordinator handles study logistics and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

What are the key skills and qualifications needed to thrive as a Part Time Clinical Data Manager, and why are they important?

To thrive as a Part Time Clinical Data Manager, you need a background in life sciences or a related field, experience with clinical data management, and attention to detail. Familiarity with data management systems like Medidata Rave, Oracle Clinical, and knowledge of regulatory standards such as GCP and CDISC are typically required. Strong organizational skills, problem-solving, and effective communication are valuable soft skills in this position. These competencies ensure accurate data collection, regulatory compliance, and successful collaboration within clinical research teams.

How do part-time Clinical Data Managers typically balance project deadlines and workload with a reduced schedule?

Part-time Clinical Data Managers often work closely with project leads to prioritize tasks and ensure that critical deadlines are met despite fewer working hours. Effective time management, clear communication, and leveraging project management tools are key strategies in this role. Collaboration with full-time team members is essential to maintain data quality and project continuity. Employers generally provide flexible work arrangements and may assign specific portions of projects that align with the part-time schedule, enabling a manageable workload while still contributing significantly to clinical research outcomes.
What are popular job titles related to Part Time Clinical Data Manager jobs in Kansas? For Part Time Clinical Data Manager jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Part Time Clinical Data Manager jobs in Kansas look for? The top searched job categories for Part Time Clinical Data Manager jobs in Kansas are:
Part Time Clinical Data Manager jobs near you
Infographic showing various Part Time Clinical Data Manager job openings in Kansas as of July 2026, with employment types broken down into 100% Part Time. Highlights an 96% In-person, and 4% Remote job distribution, with an average salary of $98,127 per year, or $47.2 per hour.

Clinical Research Coordinator

IQVIA

Wichita, KS • On-site

$35 - $42/hr

Part-time

Medical, Life

This job post has expired today. Applications are no longer accepted.

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

59th of 220 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

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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