2

Part Time Ppd Clinical Research Jobs (NOW HIRING)

next page

Showing results 1-20

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 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 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:

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 Nurse - per diem

Las Vegas, NV • On-site

Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees

Part-time

Posted 5 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 431 frontline employees who took The Breakroom Quiz


Job description

Work Schedule

Flex 12 hr shift/days

Environmental Conditions

Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Join us as a Clinical Research Nurse - And take charge of overseeing nursing staff, coordinating patient care, managing day-to-day clinical operations, ensuring adherence to healthcare standards, and fostering a collaborative and efficient work environment. This position requires the applicant to maintain a minimum scheduling availability of 2 weekend shifts a month, and 1 shift a week.
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.
What You’ll Do:
• Review inclusion/exclusion criteria with patients to ensure eligibility to participate in study. Interact with Principal Investigator for inclusion/exclusion
review of patient data. Review and witness the consenting process for subjects. Prepare study-specific documents for applicable study visit.
• Ensure the safety of patients by monitoring and assessing AEs, if any, and communicating potentially serious findings to investigators.
• Perform all procedures in the treatment areas (i.e., check-ins, gauze management, administration of drug, blood draws, ECGs, vital signs, etc.).
• Monitor staff to assure adherence to GCP, ICH, FDA, and OSHA guidelines.
• Attend initiation meetings when necessary to obtain study process clarification.
• Monitor and continuously evaluates the overall research experience of each patient to assure a positive experience.
• Perform other study-related duties as qualified by documented training.
Education and Experience:
• ADN from an accredited institution/active RN or LVN licence to practice
• 1 year experience as RN or LVN
• Technical positions may require a certificate
• Previous experience to provides the knowledge, skills, and abilities to perform the job (comparable to at least 6 years). Bachelor’s degree preferred.
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 and Abilities:
• Ability to work well in a team environment and interact with all levels of staff, clients, and subjects in a positive and professional manner
• Strong planning and organizational capabilities to manage multiple tasks and study groups at one time
• Basic computer skills, good handwriting and attention to detail
• Willingness and ability to administer investigational drugs or test investigational devices intravenously, topically, or by other approved methods of dosing
• Willingness and ability to learn and perform a variety of technical procedures such as drawing blood, processing and harvesting lab specimens, taking vital signs, performing ECGs, etc.
• Excellent verbal and written communication skills. • Ability to respond to medical emergency scenarios, in accordance with ACLS guidance, established emergency protocols, and Investigator instructions
Working Conditions and Environment:
• Work is performed in an office or clinical environment with exposure to electrical office equipment
• Occasional drives to site locations. Potential Occasional travel required
• Frequent long hours, weekends and/or holidays
• Exposure to blood and biohazardous waste
• Be available by cell phone after hours
• Exposure to fluctuating and/or extreme temperatures on rare occasions
Physical Requirements:
• Frequently stationary for 4-6 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.
• May interact with others, relating and gathering sensitive information. Interaction includes diverse groups.
• Works with guidance or reliance on oral or written instructions from management. May require 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.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthrough.


What Thermo Fisher Scientific employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom