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Picture-in-PictureFullscreenThis is a modal window.Beginning of dialog window. Escape will cancel and close the window.TextColorWhiteBlackRedGreenBlueYellowMagentaCyanOpacityOpaqueSemi-TransparentText BackgroundColorBlackWhiteRedGreenBlueYellowMagentaCyanOpacityOpaqueSemi-TransparentTransparentCaption Area BackgroundColorBlackWhiteRedGreenBlueYellowMagentaCyanOpacityTransparentSemi-TransparentOpaqueFont Size50%75%100%125%150%175%200%300%400%Text Edge StyleNoneRaisedDepressedUniformDrop shadowFont FamilyProportional Sans-SerifMonospace Sans-SerifProportional SerifMonospace SerifCasualScriptSmall CapsResetDoneClose Modal DialogEnd of dialog window.ApplyJob TypePart-time, TemporaryDescriptionAre 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, WAType: Part-Time (30 hours per week), Temporary (6-months) | HybridThis 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
Apply Today
Be part of a team that’s advancing science and improving lives.
