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Part Time Ppd Clinical Research Jobs (NOW HIRING)

IQVIA

Clinical Research Coordinator

Jefferson City, MO · On-site

$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 ...

IQVIA

Clinical Research Coordinator

Union, SC · On-site

$35 - $42/hr

Clinical Research Coordinator - Union, SC Work Set-Up: On-site Schedule Weekly Hours: 24 hours/week ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Main Line Health

Clinical Research Coord II

Wynnewood, PA · Hybrid

$23.25 - $31/hr

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... Clinical Research Coordinator II Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

Main Line Health

Clinical Research Coord II

Wynnewood, PA · Hybrid

$23.25 - $31/hr

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... Clinical Research Coordinator II Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

Main Line Health

Clinical Research Coord II

Wynnewood, PA · On-site

$23.25 - $31/hr

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... Clinical Research Coordinator II Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

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Part Time Ppd Clinical Research information

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

As of Sep 14, 2026, the average hourly pay for part time ppd clinical research 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 PPD clinical research?

A Part Time PPD Clinical Research job involves assisting with the planning, coordination, and execution of clinical trials for pharmaceutical or healthcare organizations, typically under the company PPD (Pharmaceutical Product Development). Employees in this role may perform tasks such as data collection, patient recruitment, documentation, and regulatory compliance, all while working less than full-time hours. These positions are ideal for those who require a flexible schedule but want to contribute to important medical research. Part-time roles may be suitable for students, professionals seeking work-life balance, or individuals transitioning into the clinical research field.

What does a part time PPD clinical research professional do?

A typical week for a Part Time PPD Clinical Research professional involves coordinating and conducting clinical study visits, ensuring accurate data collection, and maintaining regulatory compliance. You will often work closely with principal investigators, study coordinators, and laboratory staff to ensure study protocols are followed and participant safety is prioritized. Collaboration is essential, as you'll attend team meetings, discuss findings, and help resolve any issues that arise during trials. Flexibility is important, as schedules may vary based on study needs and participant availability.

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

To thrive as a Part Time PPD Clinical Research professional, you typically need a background in life sciences or healthcare, attention to detail, and an understanding of clinical trial protocols and regulations. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and proficiency in Microsoft Office are commonly required. Strong organizational skills, clear communication, and the ability to work independently are standout soft skills for this role. These competencies ensure accurate data collection, regulatory compliance, and effective collaboration, which are critical to the success of clinical research studies.

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

AspectPart Time Ppd Clinical ResearchPart 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; certifications like CCRP or CRC are common
Work EnvironmentWorks on clinical trial sites or remotely, often with pharmaceutical companies or CROsWorks directly at clinical trial sites, coordinating activities and patient interactions
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutionsCommonly employed by hospitals, research centers, and CROs

Both roles involve clinical trial activities and require similar educational backgrounds and certifications. However, Part Time Ppd Clinical Research often focuses on supporting multiple trials remotely or at sites, while Part Time Clinical Research Coordinators manage day-to-day trial operations and patient interactions directly at research sites.

More about Part Time Ppd Clinical Research jobs

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

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

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

The most popular types of Ppd Clinical Research jobs are:

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

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

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

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

Part Time Ppd Clinical Research jobs near you
Infographic showing various Part Time Ppd Clinical Research job openings in the United States as of September 2026, with employment types broken down into 3% As Needed, 73% Full Time, 16% Part Time, and 8% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Coordinator

Jefferson City, MO • On-site

IQVIA
Health Care and Social Assistance • 10K+ employees
Learn more about IQVIAexternal

$35 - $42/hr

Part-time

Medical, Life

Re-posted 9 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

Job description

Clinical Research Coordinator - Jefferson City, MO

Work Set-Up: On-site
Schedule 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 Clinical Research Coordinator (CRC) 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 a variety of clinical procedures, including ECG, sample collection, and vital signs.

  • Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.

  • Support study conducts by preparing study materials, setting up equipment, and planning logistical activities.

  • Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.

  • Collect and accurately record clinical data in case report forms (CRFs).

  • Collaborate with investigators and monitors, addressing queries and ensuring data quality.

  • Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Qualifications

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

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

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

  • Strong attention to detail and ability to establish effective working relationships.

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

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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