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Part Time Clinical Research Coordinator Jobs (NOW HIRING)

The Pennsylvania State University

$23.75 - $31.75/hr

Kristina Petersen's labin the Department of Nutritional Sciences is seekinga part-time Clinical Research Coordinator to support externally funded clinical trials investigating dietary interventions ...

Wisconsin

Clinical Research Coordinator

Madison, WI

$24.50 - $32.50/hr

  • Retirement

  • PTO

Clinical Research Coordinator I Job Summary: Want to join a fun, hard-working, collaborative team ... This position is full or part-time, 90%-100% * This position may require some work to be performed ...

Main Line Health

Clinical Research Coord I

Wynnewood, PA · On-site

$23.25 - $31/hr

  • PTO

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 II

Wynnewood, PA

$23.25 - $31/hr

  • PTO

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... Clinical Research Coordinator II 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

  • PTO

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 ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

  • Medical

  • Life

Clinical Research Coordinator (CRC) - Raleigh, NC Location: Raleigh, NC Work Setup ... On-site Schedule: 24 hours per week (Part-Time) About IQVIA IQVIA is a global leader in advanced ...

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

As of Aug 15, 2026, the average hourly pay for part time clinical research coordinator in the United States is $28.69, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $31.01 per hour, depending on experience, location, and employer.

What does the typical work schedule and team structure look like for a part time clinical research coordinator?

Part Time Clinical Research Coordinators often work flexible hours, which may include mornings, afternoons, or occasional evenings, depending on the needs of clinical trials and participant availability. You will usually be part of a research team comprising Principal Investigators, nurses, and other coordinators, with regular meetings to discuss trial progress and address challenges. While much of your work may be independent—like managing study documentation, scheduling participant visits, and data entry—you will frequently collaborate with other staff to ensure accurate protocol implementation and regulatory compliance. This balance allows for both autonomy and teamwork, making it well-suited to professionals seeking part-time clinical experience.

What are the key skills and qualifications needed to thrive in the part time clinical research coordinator position, and why are they important?

To succeed as a Part Time Clinical Research Coordinator, you typically need a background in health sciences or a related field, strong organizational skills, and experience with clinical research protocols. Familiarity with regulatory compliance, clinical trial management systems (CTMS), and certifications such as CCRC or ACRP are often required. Attention to detail, excellent communication, and the ability to multitask set top candidates apart in this role. These skills ensure accurate data collection, regulatory adherence, and effective collaboration with research teams, which are critical for successful trial outcomes.

What is a part time clinical research coordinator?

A Part-Time Clinical Research Coordinator (CRC) is responsible for assisting in the management and execution of clinical trials while working fewer hours than a full-time CRC. They help recruit and screen participants, collect and document data, ensure compliance with regulatory guidelines, and coordinate with investigators and sponsors. The position requires strong organizational skills, attention to detail, and knowledge of clinical research protocols. Part-time CRCs may work in hospitals, universities, or private research institutions, depending on the study. This role is ideal for those seeking flexibility while contributing to medical research.

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Part Time Clinical Research Coordinator jobs near you
Infographic showing various Part Time Clinical Research Coordinator 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 $59,666 per year, or $28.7 per hour.

Part Time Clinical Research Coordinator

SerenaGroup

Monroeville, PA • On-site

$53K - $58K/yr

Part-time

Re-posted 2 days ago

Job description

Job Type
Part-time
Description
The Clinical Research Coordinator (CRC) at SerenaGroup plays a critical role in the execution of clinical trials focused on advanced wound care and hyperbaric medicine. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory guidelines, and supporting high-quality patient care and data integrity throughout the study lifecycle.
The CRC will work collaboratively with Principal Investigators, Clinical Trial Leads, sponsors, and cross-functional teams to ensure studies are conducted efficiently, ethically, and in alignment with SerenaGroup's commitment to evidence-based care and improved patient outcomes.
Key Responsibilities
Study Coordination & Execution
  • Coordinate and manage day-to-day clinical trial activities from study start-up through close-out
  • Schedule and conduct study visits in accordance with protocol requirements
  • Ensure proper informed consent is obtained and documented for all study participants
  • Maintain accurate and up-to-date study documentation, including regulatory binders and source documents

Patient Care & Engagement
  • Identify, recruit, and screen eligible patients for clinical trials
  • Educate patients on study protocols, procedures, and expectations
  • Monitor patient safety and report adverse events in accordance with regulatory requirements

Data Management & Compliance
  • Accurately collect, record, and enter study data into electronic data capture (EDC) systems
  • Perform source data verification (SDV) and ensure data integrity and completeness
  • Ensure compliance with FDA regulations, ICH-GCP guidelines, and SerenaGroup SOPs

Collaboration & Communication
  • Serve as a liaison between investigators, sponsors, CROs, and internal teams
  • Support monitoring visits, audits, and regulatory inspections
  • Communicate effectively with cross-functional teams to ensure study milestones are met

Qualifications
Education & Experience
  • Bachelor's degree in life sciences, healthcare, or related field preferred
  • 1-3 years of experience in clinical research or healthcare setting (wound care experience a plus)
  • Experience working with clinical trial protocols and regulatory requirements preferred

Skills & Competencies
  • Strong organizational and time management skills
  • High attention to detail and accuracy in documentation
  • Excellent interpersonal and communication skills
  • Ability to manage multiple studies and priorities in a fast-paced environment
  • Proficiency in EDC systems and Microsoft Office Suite

Preferred Qualifications
  • Certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA)
  • Experience in wound care, hyperbaric medicine, or related therapeutic areas
  • Familiarity with clinical trial start-up and regulatory submissions

Salary Description
$53,000-$58,000

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