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Part Time Clinical Research Associate Jobs in Missouri

Washington University of St. Louis

$23.63 - $35.49/hr

Analytical Solutions, Big Data Analytics, Clinical Support, Communication, Computer Literacy, Data Management, Interpersonal Relationships, Organizational Leadership, Public Health Research ...

Washington University of St. Louis

$60K - $99K/yr

Clinical/diagnostic equipment. The above statements are intended to describe the general nature and ... Associate degree - Nursing Certifications/Professional Licenses: The list below may include all ...

IQVIA

Clinical Nurse Educator (per diem)

Saint Louis, MO · On-site

$40 - $45/hr

RequiredQualifications: * RN Degree - Associates required, Bachelor's preferred * Active and ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

IQVIA

MedTech

Saint Louis, MO · On-site

$39 - $42/hr

IQVIA is a leading global provider of clinical research services, commercial insights and health ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

MedTech

Kansas City, MO · On-site

$39 - $42/hr

IQVIA is a leading global provider of clinical research services, commercial insights and health ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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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

$38

$65

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

As of Sep 8, 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 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $80,239 per year, or $38.6 per hour.

Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Missouri

IQVIA

Columbia, MO • Remote

Part-time

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

63rd of 226 rated it services

Job description

Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Missouri

Location: Remote in United States

Job Type: Per Diem

About the Opportunity

Are you a Registered Dietitian seeking a flexible and meaningful role in clinical research?

IQVIA, a global leader in advancing healthcare and clinical research, is seeking experienced Registered Dietitians to support patients participating in clinical trials. This remote role focuses on delivering highquality nutrition assessments and counseling, particularly for individuals living with rare and complex conditions.

This position is ideal for clinicians who want to leverage their expertise in a telehealth environment, contribute to innovative research, and earn supplemental income while maintaining flexibility.

Key Responsibilities

As a Remote Registered Dietitian, you will:

  • Conduct nutritional assessments via telehealth and develop individualized dietetic care plans for patients with varying disease classifications

  • Provide ongoing dietary counseling and education to patients and their families

  • Deliver nutrition services only to patients in states where you are licensed to practice

  • Support patients enrolled in clinical research studies by monitoring nutritional progress and adherence

  • Maintain accurate, timely, and confidential clinical documentation

  • Participate in virtual team meetings, training sessions, and studyrelated activities

Qualifications

  • Credentialed Registered Dietitian (CDR) with current national registration

  • Active, unrestricted state licensure (except CA, MI, NJ, AZ, VA, and CO)

  • Minimum 1 year of experience providing nutrition planning and patient coaching

  • Minimum 1 year of experience delivering care remotely via telehealth

  • Strong communication and interpersonal skills

  • Experience working with patients with obesity, with or without diabetes (preferred)

  • Experience managing patients on GLP1 therapies (preferred)

  • SpanishEnglish bilingual proficiency is required.

Why Join IQVIA?

  • Flexible per diem schedule that fits your lifestyle

  • Opportunity to gain exposure to clinical trials and researchfocused care

  • Competitive supplemental income

  • Be part of a global organization advancing innovation and patient outcomes

Additional Information

  • This position is not eligible for visa sponsorship.

Ready to make a meaningful impact from anywhere?
Apply today and help support patients while contributing to the future of healthcare research.

#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 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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