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Part Time Clinical Research Associate Jobs in Seattle, WA

Uw

Research Study Assistant

Seattle, WA · On-site

$21.70/hr

Reporting to David Horn, Associate Professor of Otolaryngology-Head and Neck Surgery, the Research Study Assistant supports clinical research by assisting with participant visits, data collection ...

IQVIA

MedTech

Seattle, WA · On-site

$36 - $38/hr

... clinical research services to the life sciences industry. We believe in pushing the boundaries of ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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All JobsClinical Research Associate JobsPart Time Clinical Research Associate JobsPart Time Clinical Research Associate Jobs in Seattle, WA

Part Time Clinical Research Associate information

See Seattle, WA salary details

$13

$46

$79

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

As of Aug 24, 2026, the average hourly pay for part time clinical research associate in Seattle, WA is $46.80, according to ZipRecruiter salary data. Most workers in this role earn between $32.84 and $59.90 per hour, depending on experience, location, and employer.

What is a part time clinical research associate?

Part-time Clinical Research Associates (CRAs) are professionals who monitor and manage clinical trials on a flexible or reduced-hour schedule, rather than full-time. They are responsible for ensuring that studies comply with regulatory requirements, collecting data, and acting as a liaison between clinical trial sites and sponsors. Part-time CRAs may work remotely or travel to research sites as needed, and their schedules can vary depending on the needs of the research project. This role is ideal for those seeking work-life balance or supplementing other professional activities. Their work is critical in advancing medical research and ensuring patient safety.

What are the key skills and qualifications needed to thrive as a part time clinical research associate?

To thrive as a Part Time Clinical Research Associate, you need a background in life sciences or healthcare, knowledge of clinical research protocols, and often a bachelor’s degree in a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certification such as ACRP or SOCRA is highly valued. Strong attention to detail, organizational skills, and effective communication are essential soft skills for monitoring trials and collaborating with research teams. These skills ensure regulatory compliance, accurate data collection, and efficient trial execution, all critical for successful clinical research outcomes.

What are some common challenges faced by part time clinical research associates, and how can they be managed effectively?

Part-time Clinical Research Associates (CRAs) often face the challenge of balancing multiple study sites and projects within limited working hours. Time management and clear communication with both the research team and site staff are crucial to ensure all monitoring visits, documentation, and regulatory requirements are met on schedule. Additionally, part-time CRAs may need to be proactive in staying updated on study protocols and industry regulations, as they may not be present for all in-person team meetings. Establishing structured routines and leveraging digital tools for remote collaboration can help manage these challenges effectively.

What is the difference between Part Time Clinical Research Associate vs Clinical Research Coordinator?

AspectPart Time Clinical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often certifications like CCRP or RACBachelor's degree, often certifications like CCRP or RAC
Work EnvironmentMonitoring clinical trials at sites, remote or onsiteManaging trial operations at research sites
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinics
Search & Comparison IntentUnderstanding monitoring roles in trialsManaging trial activities at sites

Part Time Clinical Research Associates primarily focus on monitoring clinical trial progress, ensuring compliance, and verifying data accuracy, often working remotely or onsite. Clinical Research Coordinators handle the day-to-day operations at research sites, including patient recruitment and data collection. Both roles require similar credentials but differ in responsibilities and work settings.

What are popular job titles related to Part Time Clinical Research Associate jobs in Seattle, WA?

For Part Time Clinical Research Associate jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Part Time Clinical Research Associate jobs in Seattle, WA look for?

The top searched job categories for Part Time Clinical Research Associate jobs in Seattle, WA are:

What cities near Seattle, WA are hiring for Part Time Clinical Research Associate jobs?

Cities near Seattle, WA with the most Part Time Clinical Research Associate job openings:

Part Time Clinical Research Associate jobs near you
Infographic showing various Part Time Clinical Research Associate job openings in Seattle, WA as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $97,349 per year, or $46.8 per hour.

Research Associate III (Part-Time)

Seattle, WA • On-site

Inbios International Inc
Biotechnology Research and Development • 51 - 200 employees
Learn more about Inbios International Incexternal

$30.80 - $44.66/hr

Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Job description

Job Type
Part-time, Temporary
Description
About the Opportunity
We are seeking a highly motivated and experienced Research Associate III to join our team supporting the development and manufacturing of innovative molecular diagnostic assays. This position offers the opportunity to work in a collaborative, fast-paced environment supporting both research and commercial assay development.
The ideal candidate will have demonstrated expertise in molecular biology techniques, including PCR assay development, nucleic acid extraction technologies, and the analysis and interpretation of experimental data. Experience with assay optimization, troubleshooting, and data-driven decision-making is highly desirable.. That candidate is scientifically curious, detail-oriented, and passionate about advancing molecular diagnostic technologies, and work effectively collaborating with multidisciplinary teams while maintaining high standards and scientific rigor and documentation.
This is a regular, part-time employment position (two 8-hour days per week) that will be supported by project-based funding. The anticipated duration of the funded project is approximately one (1) year. While InBios hopes to retain successful team members beyond the initial project period, continued employment will depend on business needs, project requirements, and the availability of future funding through contract renewals, expanded programs, or new initiatives.
About Us
InBios International Inc. has been advancing diagnostic solutions since 1996, specializing in the design, development, and manufacturing of assays for emerging infectious diseases and biothreats. Our work supports global health initiatives and government-funded programs, with a strong focus on innovation, quality, and compliance.
Based in Seattle, WA, we offer a collaborative, mission-driven culture where employees contribute to meaningful work that impacts lives worldwide.
About the Position
  • Position Title: Research Associate III
  • Location: Seattle, WA
  • Employment Type: Part-time, nonexempt On-site
  • Position Pay Range: $30.80 - $44.66 per hour (based on knowledge, skills, and experience)
What You'll Do
  • Design, develop, optimize, and validate multiplex qPCR diagnostic assays.
  • Perform nucleic acid extraction from BSL-2 human clinical specimens containing a broad range of human pathogens using manual and automated workflows.
  • Conduct analytical and clinical validation studies to evaluate qPCR assay performance using human clinical samples.
  • Analyze experimental data, interpret results, and prepare technical reports and study documentation.
  • Perform in-house reference testing to support assay development, validation, and quality activities.
  • Collaborate with the antibody engineering team to support the discovery and screening of novel binders.
  • Maintain accurate laboratory records and ensure compliance with established laboratory procedures, quality standards, and biosafety requirements.
What We're Looking For
Required for the position:
  • Master's degree in Molecular Biology, Biochemistry, Microbiology, Biotechnology, or a related scientific discipline.
  • Minimum of two (2) years of industry experience in molecular diagnostics, biotechnology, life sciences, or a related field.
  • Experience in primer and probe design, assay development, and DNA/RNA sequence analysis.
  • Experienced in multiple PCR platforms and chemistry, including qPCR, as well as automated nucleic acid extraction systems and PCR automation/robotics.
  • Experience with BSL-2 level pathogens and human clinical samples
  • Exceptional analytical and problem-solving skills with the proven ability to think strategically.
Preferred for the position
  • Experience designing, executing, and documenting analytical and clinical studies to support FDA EUA or 510K submissions.
  • Hands-on experience with mammalian cell culture.
Work Environment
  • GMP-compliant manufacturing and laboratory setting
  • Biosafety Level 2 (BSL-2) environment handling potentially infectious materials
  • Use of personal protective equipment (PPE), including gloves, lab coats, and eye protection
  • Work may include standing for extended periods and handling biological materials
Perks & Benefits
  • This part-time position is not eligible for employer-sponsored group insurance (which includes medical, dental, vision, life, and other voluntary coverage options as well as FSA.) Washington Paid Sick Leave and other legally required benefits apply.
  • 401(k) + Roth IRA + FSA options
  • Part-time employees receive a prorated PTO benefit equivalent to the full-time policy, which includes two weeks of paid vacation and 11 paid holidays (including the annual winter break)
  • Competitive pay and growth opportunities
  • Supportive, team-oriented culture focused on innovation and impact
Apply Today
Bring your expertise in molecular diagnostics, qPCR assay development, and infectious disease testing to a collaborative upstream team developing next-generation diagnostic solutions that improve health outcomes worldwide.

Apply