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Part Time Ppd Clinical Research Jobs (NOW HIRING)

Access Community Clinical Trials

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Clinical Research Nurse

Abilene, TX · On-site

Abilene, Texas Employment Type: Part-Time Access Community Clinical Trials (ACCT) is a growing clinical research organization dedicated to expanding access to high-quality clinical trials within ...

IQVIA

Clinical Research Coordinator

Oxford, MS

$35 - $42/hr

On-site Scheduled Weekly Hours: 16 hours per week Position Type: Part-time About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We work ...

IQVIA

Clinical Research Coordinator

Wichita, KS

$35 - $42/hr

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 ...

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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 Jun 15, 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 typical week look like for a Part Time PPD Clinical Research professional, and how do they collaborate with other team members?

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 job?

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, and why are they important?

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:
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Part Time Ppd Clinical Research jobs near you
Infographic showing various Part Time Ppd Clinical Research job openings in the United States as of June 2026, with employment types broken down into 76% Full Time, 9% Part Time, and 15% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.
Clinical Research Physician(Gen Med) - Part Time Opportunity!

Clinical Research Physician(Gen Med) - Part Time Opportunity!

Thermo Fisher Scientific

Atlanta, GA • On-site

Part-time

Posted 26 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 398 frontline employees who took The Breakroom Quiz

188th of 518 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on- now and in the future.
Location/Division Specific Information:
Trialmed helps biopharmaceutical companies overcome patient enrollment and research site challenges by combining a powerful patient recruiting solution with more than 150 clinical research sites located throughout the world. As a business of PPD, we are committed to optimizing each step in the patient journey and delivering best-in-class site performance to bring our customers
greater certainty to clinical trial delivery.
*Must be legally authorized to work in the United States without sponsorship.
*Must be able to pass a comprehensive background check, which includes a drug screening.
Gen Med Hours: 4 days/week with approx. 3 hours/day. Some flexibility around days/hours might be able to be accommodated.
Discover Impactful Work:
Conducts all clinical trials (studies) according to ICH GCP, local regulations, study protocol and company processes. Ensures the medical wellbeing and safety of the participants through the safe performance and execution of the studies. Maintains clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site which includes: recruitment, enrolment and retention of study participants.
A day in the Life:
  • Carries out clinical evaluation and assessment of participants to ensure eligible participants are enrolled onto studies.
  • Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety and retention of participants.
  • Interprets protocols and IB and participate in initiatives to strategize for patient recruitment.
  • Ensures and protect the welfare and safety of participants through ethical conduct; this should receive the highest priority at all times during all aspects of the study.
  • Fulfills and comply with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations.
  • Reports any safety threats, that may impact stakeholders/participants and action complaints or QIs as per site processes.
  • Exercises meticulous attention to detail in recording information and source management.
  • Actively involved in audit preparations and site inspections.
  • Oversees the management of investigational medical product (IMP).

Keys to Success:
  • A valid medical degree and registration within the country of practice
  • A medical license in good standing, with unrestricted ability to practice in place of work, where applicable
  • A valid ICH GCP certificate(can be obtained after employment)
  • Exceptional general medical practitioner diagnosis and treatment proficiency
  • At least one-year experience working in clinical research, or comparable research/clinical expertise to demonstrate the ability to work in clinical trials

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills, Abilities
  • Good understanding of medical terminology, drug safety, and interpretation of lab reports
  • Computer proficiency and confident in using Microsoft Office and other sponsor related programs and portals
  • Good administration skills and a passion for quality and detail
  • Comprehensive attention to detail
  • Capable of working well under pressure and meeting deadlines
  • Good understanding of commercial and financial concepts and the impact thereof on the business
  • Capable of consistently working well with others and assisting in other areas as needed
  • Capable of learning new processes and systems quickly
  • Strong cognitive skills, with the ability to think, read, learn, reason, interpret and pay attention to detail in daily operations and tasks
  • Capable of working independently
  • Good prioritization and multitasking skills

Physical Requirements / Work Environment
  • Frequently stationary for 4-8 hours per day.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
  • Frequent mobility required.
  • Occasional crouching, stooping, bending and twisting of upper body and neck.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Ability to access and use a variety of computer software developed both in-house and off the-shelf.
  • Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
  • Frequently interacts with others to obtain or relate information to diverse groups.
  • Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
  • Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress.
  • Ability to multi-task.
  • Regular and consistent attendance.

Thermo Fisher Scientific offers employment with an innovative, forward thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

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