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Temporary Clinical Research Jobs in Bothell, WA (NOW HIRING)

Uw

Research Coordinator 1

Seattle, WA · On-site

$90K/yr

... clinical research studies focused on lung infection, inflammation, and immunity in the ... First Shift (United States of America) Temporary or Regular? This is a regular position FTE ...

Uw

Research Coordinator 1

Seattle, WA · On-site

$90K/yr

Collect and record clinical data from a combination of electronic medical record systems review ... First Shift (United States of America) Temporary or Regular? This is a regular position FTE ...

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How much do temporary clinical research jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for temporary clinical research in Bothell, WA is $45.97, according to ZipRecruiter salary data. Most workers in this role earn between $32.26 and $58.85 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Temporary Clinical Research position, and why are they important?

To excel in Temporary Clinical Research, candidates typically need a background in life sciences or healthcare, familiarity with clinical trial protocols, and attention to regulatory compliance. Experience with data collection software, electronic data capture (EDC) systems, and Good Clinical Practice (GCP) certification are highly valuable. Strong organizational, communication, and problem-solving skills help professionals adapt quickly and contribute effectively in temporary project-based settings. These abilities ensure accurate, ethical research conduct and seamless integration with research teams, even on short-term assignments.

What is a Temporary Clinical Research job?

A Temporary Clinical Research job involves assisting in medical or scientific studies for a limited period. Responsibilities may include data collection, patient interaction, regulatory compliance, and administrative support. These roles are often project-based and may be available in hospitals, universities, or pharmaceutical companies. Temporary positions allow professionals to gain experience in clinical research without committing to a long-term role.

What are the typical responsibilities of someone working in a Temporary Clinical Research position?

In a Temporary Clinical Research role, you can expect to assist with tasks such as collecting and managing study data, coordinating participant visits, and ensuring compliance with study protocols. You may also help with regulatory documentation, support the recruitment of research subjects, and collaborate closely with investigators, sponsors, and other research team members. Since these positions are project-based, you’ll need to adapt quickly to new environments and processes. This role provides valuable hands-on experience in clinical research, and can be a great stepping stone for those aiming to advance to permanent or higher-level positions in the field.

What are the most commonly searched types of Clinical Research jobs in Bothell, WA? The most popular types of Clinical Research jobs in Bothell, WA are:
What job categories do people searching Temporary Clinical Research jobs in Bothell, WA look for? The top searched job categories for Temporary Clinical Research jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Temporary Clinical Research jobs? Cities near Bothell, WA with the most Temporary Clinical Research job openings:
Temporary Clinical Research jobs near you
Clinical Research Coordinator I (Temporary/Part-Time)

Clinical Research Coordinator I (Temporary/Part-Time)

Inbios International Inc

Seattle, WA • On-site

$26.44 - $31.25/hr

Part-time

Medical, Dental, Vision, Life, Retirement

Re-posted 4 days ago

Job description

Job Type
Part-time, Temporary
Description
Are you a detail-oriented problem-solver with a passion for purpose-driven work? Join InBios, a mission-focused biotech company developing diagnostic tools that combat infectious diseases worldwide.
About Us
InBios International Inc. has been in business since 1996 designing and manufacturing diagnostic assays for emerging infectious diseases and biothreats. Our work supports global health initiatives and government-funded research, with a strong emphasis on innovation, quality, and compliance. Based in Seattle, we offer a collaborative culture, competitive compensation, and meaningful work that makes a global impact.
Location: Seattle, WA
Type: Part-Time (30 hours per week), Temporary (6-months) Hybrid
This is a project-based position funded by a federal contract. If selected for the position, you will be hired as a temporary, part-time employee and the term of employment is dependent upon ongoing funding.
Position Wage Range: $26.44 - $31.25/per hour
What You'll Do
We're looking for a temporary, part-time Clinical Research Coordinator to support clinical studies and international product registration. The successful candidate must have a BS in a scientific discipline, have familiarity with Good Clinical Practice (GCP) and have excellent attention to details as well as good communication skills but written and verbal.
Key Responsibilities
Clinical Site Monitoring
  • Under the direction of the Project Manager assist in the maintenance of regulatory binders and Institutional Review Board (IRB) submissions.
  • Monitor clinical study to ensure that all participant records entered into the electronic data capture system are accurate and follow the clinical protocol and source documents.
  • Participate in Site Initiation training (SIV), monitor study compliance, and assist with study closeout.
  • Ensure that participants enrolled in the study meet the inclusion/exclusion criteria.
  • Monitor and report protocol deviations and adverse events in a timely manner.
  • Participate in study site close-out.
Product Registrations (International)
  • Identify regulatory requirements for product registrations worldwide.
  • Review analytical and clinical data against country regulatory requirements and identify gaps that need to be filled to obtain product registration.
  • Assist in the preparation of technical files in compliance with IVDR.
What We're Looking For
Required
  • Bachelor's degree in a scientific discipline.
  • Strong attention to detail, excellent written and verbal communication, and proficiency with technology (e.g., MS Office, Electronic Database Systems).
  • Knowledge of ICH GCP guidelines. GCP certification.
  • Entry-level knowledge of IVDR requirements for medical devices.
Preferred
  • 1- to 3-year experience in project management.
  • Certified Clinical Research Associate credential.
Perks & Benefits
  • Medical, dental, vision, life & disability insurance
  • 401(k) + Roth IRA + FSA
  • Prorated paid holidays and sick time as applicable to term of employment and work schedule in accordance with policies stated in the Company's employee handbook.
  • Supportive, mission-driven culture

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