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Senior Software Engineer - Report Generation

Job in Northern, Floyd County, Kentucky, USA
Listing for: Caris Life Sciences
Full Time position
Listed on 2026-08-27
Job specializations:
  • Software Development
    Software Engineer, Software Architect
Salary/Wage Range or Industry Benchmark: 120000 - 180000 USD Yearly USD 120000.00 180000.00 YEAR
Job Description & How to Apply Below
Location: Northern

At Caris, we understand that cancer is an ugly word—a word no one wants to hear, but one that connects us all. That’s why we’re not just transforming cancer care—we’re changing lives. We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting‑edge molecular science and AI, we ask ourselves every day: “What would I do if this patient were my mom?”

That question drives everything we do. But our mission doesn’t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare—driven by innovation, compassion, and purpose. Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.

Position

Summary

Caris Life Sciences serves hundreds of thousands of molecular cases a year and continues to grow at double‑digit rates. Its molecular, imaging, and clinical‑outcomes data support software that helps ensure a cancer patient’s report is right, complete, and on time.

The Senior Software Engineer - Clinical Software Products delivers senior‑level engineering across Caris’s clinical application portfolio: product delivery, reliability, and incremental modernization of the production systems that support regulated clinical workflows. This assignment supports report generation and template capabilities for clinical result documents. Engineers deliver report types, template enhancements, and rendering‑pipeline improvements while maintaining reliability, traceability, and change‑control discipline.

The engineering environment supports advanced AI coding assistants and agentic workflows across design, implementation, and test generation. Characterization tests and golden‑master replay validation provide executable evidence. Onboarding is harness‑first: the engineer builds or extends characterization tests to capture current behavior as repeatable validation evidence. Delivery runs on CI/CD, automated testing, application‑level observability, and risk‑based release governance aligned with current FDA Computer Software Assurance guidance.

Representative technologies across the portfolio include Java, Type Script, browser‑based application frameworks, server‑side JavaScript, and selected enterprise Java components.

The interview process covers the specific assignment and technology stack.

Reporting to an Engineering Manager or Senior Engineering Manager within Clinical Software Engineering, this senior individual contributor designs, builds, and maintains clinical software applications governed by SOX financial controls and FDA regulatory requirements. The role leads technical delivery on an assigned product team, participates in architecture and design decisions, and upholds the engineering and compliance standards those systems require.

Location:

Irving, Texas (Dallas–Fort Worth), on‑site/hybrid, minimum three days per week on campus; co‑located with Caris’s laboratory and clinical operations.

Job Responsibilities
  • Design, implement, and maintain features and components across Caris’s clinical software platforms: well‑structured, testable, documented code that holds up in a regulated production environment.
  • Lead and contribute to design and architecture discussions, laying out the technical options and trade‑offs that inform the team’s decisions.
  • Give and receive peer code review, holding code‑quality standards and surfacing issues that could affect system correctness, performance, or compliance.
  • Work with product management to sharpen requirements, name the technical constraints, and estimate backlog items.
  • Write and maintain the technical record: design documents, architecture decision records, and operational runbooks that meet SOX and FDA change‑control obligations.
  • Instrument, monitor, and support production systems; participate in incident response and root‑cause analysis for production issues.
  • Build automated test coverage across unit, integration, and end‑to‑end levels as first‑class engineering work.
  • Automate the recurring engineering…
Position Requirements
10+ Years work experience
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