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Part Time Ppd Clinical Research Jobs (NOW HIRING)

Wisconsin

Clinical Research Coordinator

Madison, WI

$24.50 - $32.50/hr

This position is full or part-time, 90%-100% * This position may require some work to be performed ... A Clinical Research Coordinator II will perform tasks more independently, collect more complex ...

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 ...

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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 Aug 19, 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?

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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 August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Coordinator (Part-time)

Prolerity Clinical Research

Somers Point, NJ • On-site

$24.75 - $32.75/hr

Part-time

Posted 19 days ago

Job description

Description:

Clinical Research Coordinator (CRC)

The Clinical Research Coordinator (CRC) is responsible for overseeing and managing the daily operational activities of assigned clinical research studies. This role works closely with investigators, clinical staff, study participants, sponsors, and CROs to ensure that all research activities are conducted in compliance with study protocols, regulatory requirements, and ethical standards.

The CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution from study start-up through close-out.

Key Responsibilities

Study Management & Coordination

  • Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out.
  • Support study start-up activities including feasibility, regulatory submissions, and site activation.
  • Attend investigator meetings, site initiation visits, and other study-related meetings.
  • Manage visit schedules and coordinate study-related activities across clinical teams.

Recruitment, Enrollment & Consent

  • Collaborate with recruitment teams to support participant screening and enrollment.
  • Conduct informed consent discussions with participants, ensuring understanding of study requirements and documentation of consent.
  • Ensure protocol and regulatory requirements are met throughout the enrollment process.

Clinical Oversight & Subject Monitoring

  • Monitor and assess study subjects in accordance with protocol requirements.
  • Identify, document, and report adverse events in collaboration with the Principal Investigator and clinical staff.
  • Escalate safety concerns and protocol issues to the PI, sponsor, and IRB as required.

Documentation, Data & Systems

  • Maintain accurate and complete source documentation, case report forms, regulatory files, and study records.
  • Enter study data into EDC and other required systems and manage study databases.
  • Complete, verify, and resolve case report forms and sponsor or monitor queries in a timely manner.
  • Report protocol deviations to the PI, sponsor, and IRB as required.

Investigational Product & Specimen Management

  • Manage investigational product accountability records and documentation.
  • Collect, process, package, and ship study specimens per protocol requirements.
  • Perform phlebotomy and handle biological specimens in accordance with study protocols and safety guidelines, when trained and authorized.

Quality, Compliance & Team Support

  • Ensure all study activities comply with SOPs, GCP, and regulatory requirements.
  • Support quality assurance activities and audit readiness.
  • Provide assistance and mentorship to fellow coordinators as needed.
  • Maintain strict confidentiality of participant and study information.

Communication & Outreach

  • Serve as the primary point of contact for sponsor and CRO communications.
  • Participate in occasional outreach or community events related to clinical trials.
  • Ensure timely, accurate communication of study updates and issues.


Additional Responsibilities

This job description outlines the primary responsibilities of the Clinical Research Coordinator but is not exhaustive. Additional duties may be assigned as needed to support study requirements, operational needs, and organizational priorities. Responsibilities may evolve based on protocol complexity and business needs.


Requirements:
  • Knowledge, Skills, and Abilities
  • • Strong leadership and communication skills
  • • Exceptional organizational and multitasking abilities
  • • High attention to detail and commitment to regulatory compliance
  • • Ability to work independently and collaboratively in a multidisciplinary environment
  • • Strong time management and operational efficiency skills
  • • Proficiency with office equipment and study-specific systems
  • • Ability to maintain strict confidentiality
  • Required Experience & Qualifications
  • • Education: Bachelor’s degree in a related field
  • • Experience: Minimum of two (2) years of clinical research or clinical trial management experience
  • • Preferred Credentials: Medical certification or licensure (e.g., MS, LPN, RN)
  • • Phlebotomy: Prior experience performing blood draws and handling biological specimens required