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Model Context Protocol Jobs in Utah (NOW HIRING)

Medical Writing Manager

Provo, UT · Remote

$50 - $80/hr

Your work will shape how models learn, reason, and perform through high-quality, real-world input ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Your work will shape how models learn, reason, and perform through high-quality, real-world input ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Your work will shape how models learn, reason, and perform through high-quality, real-world input ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Your work will shape how models learn, reason, and perform through high-quality, real-world input ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Your work will shape how models learn, reason, and perform through high-quality, real-world input ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Your work will shape how models learn, reason, and perform through high-quality, real-world input ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Your work will shape how models learn, reason, and perform through high-quality, real-world input ... Trace narrative claims to source records--tables, figures, listings, and protocols--to verify that ...

Revit/CAD Designer

Salt Lake City, UT · Hybrid

$26.25 - $36/hr

Integrate design models with GIS and other project data sources for improved project context ... and protocols. * Participate in project meetings to coordinate technical design and modeling ...

... security protocols. * Experience in government or regulated industries (e.g., public sector ... Ability to thrive in a startup-like environment within a government context, adapting to ambiguity ...

Data & Infrastructure Engineer

Draper, UT · On-site

$107K - $128K/yr

Implement and maintain data security protocols to protect WorkBay's proprietary information ... Exposure to AI/LLM architecture -- understanding how large language models consume data and how to ...

Showing results 41-60

Model Context Protocol information

What is the difference between Model Context Protocol vs Data Analyst?

AspectModel Context ProtocolData Analyst
Required CredentialsKnowledge of data modeling, API protocols, and software developmentBachelor's degree in statistics, mathematics, or related field
Work EnvironmentTechnical teams, software development, AI/ML projectsBusiness intelligence, reporting, data visualization
Industry UsageTech, AI, software developmentFinance, marketing, healthcare, business
Search & Comparison IntentUnderstanding technical protocols for AI modelsAnalyzing data for insights and decision-making

The Model Context Protocol focuses on technical data exchange and AI model integration, requiring programming and API knowledge. In contrast, Data Analysts interpret data to generate reports and insights, often working with business tools. Both roles involve data but serve different functions within organizations.

What job categories do people searching Model Context Protocol jobs in Utah look for? The top searched job categories for Model Context Protocol jobs in Utah are:
What cities in Utah are hiring for Model Context Protocol jobs? Cities in Utah with the most Model Context Protocol job openings:
Infographic showing various Model Context Protocol job openings in Utah as of August 2026, with employment types broken down into 57% Full Time, 21% Part Time, 4% Temporary, and 18% Contract. Highlights an 81% In-person, and 19% Remote job distribution.

Medical Writing Manager

micro1 AI

Provo, UT • Remote

$50 - $80/hr

Part-time

Posted 4 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.