ZipRecruiter

Log In

2

Part Time Ppd Clinical Research Jobs (NOW HIRING)

Protouch Staffing

Clinical Research Nephrologist

Arden, NC · On-site

$100 - $250/hr

Job Title: Part-Time Clinical Research Nephrologist Compensation: $100 - $250 per hour Schedule: Part-Time (0-8 hours) start date: 0-6 months About the Role We are seeking a board-certified to serve ...

Dayton Children's

Clinical Research Coordinator

Dayton, OH · On-site

$23.50 - $31.25/hr

Surgical Services Schedule: Part time Hours: 20 Job Details: The Clinical Research Coordinator will perform clinical research activities under the general direction of the Clinical Research ...

Investigator Research Network

Be Seen First

PRN Clinical Research Infusion Nurse

Leland, NC · On-site

This position is on an as-needed, part-time basis and will primarily support IV infusion visits for a clinical research trial. Responsibilities may also include other study-related duties, patient ...

IQVIA

Clinical Research Coordinator

Albuquerque, NM

$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 ...

previous pagenext page

Showing results 21-40

All JobsPart Time JobsHealthcare JobsMedical Research JobsClinical Researcher JobsPart Time Ppd Clinical Research Jobs

Part Time Ppd Clinical Research information

See salary details

$12

$41

$69

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

As of Sep 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 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.

Physician, MD/DO - Clinical Research - Part-time

El Paso, TX • On-site

Headlands Research
Scientific Research and Development Services • 51 - 200 employees
Learn more about Headlands Researchexternal

Part-time

Posted 14 days ago

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
Location: El Paso, TX | Site Name: Headlands Research - El Paso | Part-Time | Clinical Research
Join Us in Improving Lives through Clinical Research
At Headlands Research, we're not just building a clinical trial network; we are working to bring clinical trials to underserved communities and treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we've rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.
Championing Diversity in Clinical Trials
Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.
The Role of a Lifetime
Are you ready to make a difference? We're seeking an experienced physician to help us grow our clinical research site at Headlands Research - El Paso, primarily physicians with previous experience serving as a Principal Investigator (PI) or Sub-Investigator (Sub-I). We are flexible and open to considering multiple specialties, schedules, and availability. The site's hours are Mondays through Fridays from 8:00 AM - 4:30 PM.
Why Join Us?
  • Flexible Schedule: Work on your terms, with a schedule that fits your life.
  • Dynamic Team Environment: You'll help Headlands Research continue to build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you'll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.

Responsibilities:
  • Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and any protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.

Requirements:
  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without.
  • Eligible for or active unencumbered license to practice as an MD or DO within the state of Texas required
  • Must be board-certified or board-eligible.
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Apply