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Part Time Ppd Clinical Research Jobs (NOW HIRING)

IQVIA

Clinical Research Coordinator

Albuquerque, NM · On-site

$35 - $42/hr

Onsite Schedule: 24 Hours/Week (Parttime) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with leading pharmaceutical ...

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

Our commitment to excellence in clinical research operations ensures the highest standards of ... This is a part-time position that requires working one week per month on-site according to the ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

On-site Schedule: 24 hours per week (Part-Time) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare ...

IQVIA

Clinical Research Coordinator

Cincinnati, OH · On-site

$35 - $42/hr

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

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

Marietta, GA · On-site

$35 - $42/hr

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

Main Line Health

Clinical Research Coord I

Wynnewood, PA

$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 I Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

Main Line Health

Clinical Research Coord I

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 I Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

Uofl

$23.25 - $31/hr

This is a part time temporary position scheduled to work 15 hours per week. Essential Duties and Responsibilities: * Facilitates compliance with the research protocol and Good Clinical Practice ...

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All JobsPpd Clinical Research JobsPart Time Ppd Clinical Research Jobs

Part Time Ppd Clinical Research information

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$12

$41

$69

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

As of Aug 13, 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 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 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 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.

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.
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 job categories do people searching Part Time Ppd Clinical Research jobs look for?

The top searched job categories for Part Time Ppd Clinical Research jobs 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 August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Coordinator

IQVIA

Albuquerque, NM • 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

61st of 223 rated it services

Job description

Clinical Research Coordinator - Albuquerque, NM
Work SetUp: Onsite
Schedule: 24 Hours/Week (Parttime)

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with leading pharmaceutical, biotechnology, and medical device organizations to advance innovation and improve patient outcomes worldwide. Through scientific expertise, operational excellence, and cuttingedge technology, IQVIA is shaping the future of healthcare.

About the Role

IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This role is wellsuited for a detailoriented research professional who enjoys direct patient interaction, values data integrity, and is committed to highquality clinical research within diverse communities.

As a CRC, you will play a critical role in coordinating study operations, supporting patient recruitment and retention, performing studyrelated procedures, and ensuring adherence to study protocols and regulatory requirements.

Key Responsibilities

  • Coordinate and conduct clinical research activities in accordance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements

  • Perform studyrelated clinical procedures, including ECGs, vital signs, and biological sample collection

  • Conduct patient visits including screening, enrollment, education, orientation, and followup

  • Support patient recruitment efforts and community outreach, including bilingual (English/Spanish) communication

  • Prepare study materials, manage equipment setup, and support daily clinic operations

  • Accurately collect, document, and enter clinical data into electronic data capture (EDC) systems and case report forms (CRFs)

  • Request, review, and manage medical records to support study eligibility and documentation

  • Collaborate with investigators, sponsors, and monitors to address data queries and ensure study quality

  • Maintain a safe clinical environment and serve as a patient advocate throughout study participation

Qualifications

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

  • Minimum of 1+ year of clinical research coordination experience, including prior study coordination

  • Handson experience with clinical research operations, including:

    • Data entry and query resolution in EDC systems

    • Chart prescreening and patient prescreening activities

    • Conducting and coordinating patient visits

    • Patient outreach and education via phone and facetoface communication regarding clinical trials

    • Scheduling study visits and managing visit logistics

    • Collection, processing, and shipping of laboratory samples

    • Recruitment activities and participant followup

    • Regulatory document review and maintenance

  • Working knowledge of clinical trial processes, GCP guidelines, and medical terminology

  • Experience requesting and managing medical records

  • Bilingual in English and Spanish (written and verbal) is preferred but not required

  • Strong organizational skills, attention to detail, and ability to work effectively with diverse teams and patient populations

Ready to Make an Impact?

Join IQVIA and contribute to highquality clinical research that advances science while serving diverse patient communities.
Apply today and be part of a team helping bring innovative treatments to patients.

Additional Information

  • This position is not eligible for visa 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.

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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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