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Part Time Clinical Research Associate Jobs in Missouri

IQVIA

Site Research Assistant

Kansas City, MO

$25 - $39/hr

... Clinical Practice (GCP) standards. Qualifications * Associate degree preferred or equivalent ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Washington University of St. Louis

$19.93 - $29.93/hr

Location SAINT LOUIS, MO 63110 Position Summary Under direction, participates in clinical research ... Associate degree Certifications/Professional Licenses: No additional certification/professional ...

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All JobsClinical Research Associate JobsPart Time Clinical Research Associate JobsPart Time Clinical Research Associate Jobs in Missouri

Part Time Clinical Research Associate information

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$11

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$65

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

As of Aug 17, 2026, the average hourly pay for part time clinical research associate in Missouri is $38.58, according to ZipRecruiter salary data. Most workers in this role earn between $27.07 and $49.38 per hour, depending on experience, location, and employer.

What is a part time clinical research associate?

Part-time Clinical Research Associates (CRAs) are professionals who monitor and manage clinical trials on a flexible or reduced-hour schedule, rather than full-time. They are responsible for ensuring that studies comply with regulatory requirements, collecting data, and acting as a liaison between clinical trial sites and sponsors. Part-time CRAs may work remotely or travel to research sites as needed, and their schedules can vary depending on the needs of the research project. This role is ideal for those seeking work-life balance or supplementing other professional activities. Their work is critical in advancing medical research and ensuring patient safety.

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

To thrive as a Part Time Clinical Research Associate, you need a background in life sciences or healthcare, knowledge of clinical research protocols, and often a bachelor’s degree in a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certification such as ACRP or SOCRA is highly valued. Strong attention to detail, organizational skills, and effective communication are essential soft skills for monitoring trials and collaborating with research teams. These skills ensure regulatory compliance, accurate data collection, and efficient trial execution, all critical for successful clinical research outcomes.

What are some common challenges faced by part time clinical research associates, and how can they be managed effectively?

Part-time Clinical Research Associates (CRAs) often face the challenge of balancing multiple study sites and projects within limited working hours. Time management and clear communication with both the research team and site staff are crucial to ensure all monitoring visits, documentation, and regulatory requirements are met on schedule. Additionally, part-time CRAs may need to be proactive in staying updated on study protocols and industry regulations, as they may not be present for all in-person team meetings. Establishing structured routines and leveraging digital tools for remote collaboration can help manage these challenges effectively.

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

AspectPart Time Clinical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often certifications like CCRP or RACBachelor's degree, often certifications like CCRP or RAC
Work EnvironmentMonitoring clinical trials at sites, remote or onsiteManaging trial operations at research sites
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinics
Search & Comparison IntentUnderstanding monitoring roles in trialsManaging trial activities at sites

Part Time Clinical Research Associates primarily focus on monitoring clinical trial progress, ensuring compliance, and verifying data accuracy, often working remotely or onsite. Clinical Research Coordinators handle the day-to-day operations at research sites, including patient recruitment and data collection. Both roles require similar credentials but differ in responsibilities and work settings.

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

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

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

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

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

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

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

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

Part Time Clinical Research Associate jobs near you
Infographic showing various Part Time Clinical Research Associate job openings in Missouri as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $80,239 per year, or $38.6 per hour.

Site Research Assistant

IQVIA

Kansas City, MO

$25 - $39/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 224 rated it services

Job description

Research Assistant - Kansas City, MO

Work Setup: On-site
Scheduled Weekly Hours: 24 Hours/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 the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

About the Role

We are seeking a Research Assistant (RA) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.

Key Responsibilities

  • Perform accurate EDC data entry, manage queries, and ensure timely resolution.

  • Maintain and update the regulatory binder in compliance with documentation and audit standards.

  • Coordinate and schedule subject visits, procedures, and follow-up activities.

  • Build effective working relationships with investigators, clinical staff, and study team members.

  • Support subject screening, recruitment, and enrollment activities.

  • Assist with patient/research participant scheduling and collection of medical history.

  • Coordinate lab procedures and follow-up care in alignment with study protocols.

  • Ensure strict adherence to IRBapproved protocols, including assistance with informed consent processes.

  • Uphold participant safety and report concerns promptly per SOPs and Sponsor requirements.

  • Follow all company policies, SOPs, guidelines, and Good Clinical Practice (GCP) standards.

Qualifications

  • Associate degree preferred or equivalent combination of education and relevant experience.

  • 1+ years of experience in a clinical research environment preferred.

  • Strong working knowledge of clinical trials, GCP, and protocolspecific procedures.

  • Proficiency with EDC systems, data entry accuracy, and query management.

  • Experience with visit scheduling, regulatory documentation, and binder maintenance.

  • Excellent attention to detail, time management, and task prioritization.

  • Strong communication, interpersonal, and relationshipbuilding skills.

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 $25.00-$39.00 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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