Job Summary:We are seeking a detail-oriented and experienced Technical Writer. In this role, you will be responsible for developing, updating, and maintaining technicaldocumentation to support our clinician services team. You ll work closely with clinical experts,data engineers, and other key stakeholders to ensure specifications are clear, accurate, andmeet the needs of our team.Key Responsibilities: Write and edit detailed data flow diagrams based on the data platformand quality measure specifications for healthcare programs such as MIPS. Translate complex clinical and technical requirements into clear, standardizeddocumentation. Collaborate with subject matter experts, data engineers, and quality analysts to gatherand verify technical information to produce documentation for internal teams. Maintain version control of specifications and track changes across documentlifecycles. Ensure consistency, clarity, and accuracy across all documentation. Support the development of supporting materials such as implementation guides, FAQs,and change logs.Required Qualifications: 3+ years of experience in technical writing, preferably in the healthcare or qualitymeasurement space. Familiarity with healthcare quality programs such as CMS quality programs (MIPS,ACO), or similar. Excellent written and verbal communication skills, with the ability to explain complexdata to varied audiences. Proficient with Google Drive and document management tools.Preferred Qualifications: Experience in working at Healthcare Data companies Experience with clinical quality language or standards (e.g., CQL, FHIR, QDM). Understanding of measure development processes and national quality frameworks. Ability to interpret and document clinical and data logic clearly for multiple audiences
Keyskills: Version control Technical writing CMS Healthcare Document management MIPS Technical documentation