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Remote Clinical Lab Scientist Jobs in Bothell, WA

micro1 AI

Cheminformatics Specialist - Remote

Seattle, WA · Remote

$80 - $110/hr

... clinical data sources. * Provide expert insights on structure-activity and structure-property ... Assess and review AI-generated outputs for scientific rigor, accuracy, and practical relevance ...

micro1 AI

Cheminformatics Specialist - Remote

Renton, WA · Remote

$80 - $110/hr

... clinical data sources. * Provide expert insights on structure-activity and structure-property ... Assess and review AI-generated outputs for scientific rigor, accuracy, and practical relevance ...

micro1 AI

Cheminformatics Specialist - Remote

Everett, WA · Remote

$80 - $110/hr

... clinical data sources. * Provide expert insights on structure-activity and structure-property ... Assess and review AI-generated outputs for scientific rigor, accuracy, and practical relevance ...

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All JobsClinical Lab Scientist JobsRemote Clinical Lab Scientist JobsRemote Clinical Lab Scientist Jobs in Bothell, WA

Remote Clinical Lab Scientist information

See Bothell, WA salary details

$47.5K

$105.5K

$171K

How much do remote clinical lab scientist jobs pay per year?

As of Aug 14, 2026, the average yearly pay for remote clinical lab scientist in Bothell, WA is $105,550.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,000.00 and $133,000.00 per year, depending on experience, location, and employer.

How does a remote clinical lab scientist effectively collaborate with on-site laboratory teams?

Remote Clinical Lab Scientists work closely with on-site staff through secure digital platforms, such as laboratory information systems and video conferencing tools. They often participate in daily virtual meetings to discuss case findings, clarify test results, and troubleshoot technical issues. Clear communication and timely documentation are essential for ensuring that remote and on-site teams remain aligned, maintain sample integrity, and deliver accurate results to healthcare providers. Building strong relationships with on-site colleagues can also help remote scientists stay informed about any changes in lab protocols or workflows.

What is a remote clinical lab scientist?

A Remote Clinical Lab Scientist is a trained laboratory professional who performs diagnostic tests and analyzes samples, but works from a remote location rather than on-site in a laboratory. These professionals use digital tools, secure data systems, and sometimes remote-access instruments to review results, troubleshoot issues, and provide expert guidance. They play a crucial role in ensuring accurate laboratory diagnostics for patient care, collaborating with on-site teams and maintaining regulatory standards. Remote Clinical Lab Scientists often need strong communication skills and a good understanding of laboratory information systems.

What are the key skills and qualifications needed to thrive as a remote clinical lab scientist?

To thrive as a Remote Clinical Lab Scientist, you need a strong background in laboratory science, attention to detail, and typically a bachelor's degree in medical laboratory science or a related field along with relevant certification (e.g., ASCP). Familiarity with laboratory information systems (LIS), digital microscopy, and remote diagnostic platforms is essential. Excellent communication, critical thinking, and self-motivation are important soft skills for collaborating with teams and managing work independently. These skills and qualities ensure accurate, timely results and effective coordination in a remote healthcare environment.

What job categories do people searching Remote Clinical Lab Scientist jobs in Bothell, WA look for?

The top searched job categories for Remote Clinical Lab Scientist jobs in Bothell, WA are:

What cities near Bothell, WA are hiring for Remote Clinical Lab Scientist jobs?

Cities near Bothell, WA with the most Remote Clinical Lab Scientist job openings:

Remote Clinical Lab Scientist jobs near you

Medical Writer / Clinical Document Author

micro1 AI

Bellevue, WA • Remote

$50 - $80/hr

Part-time

Posted 10 days ago

Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.

Apply