Product Analyst - Clinical Software- Phoenix, AZ

Product Analyst - Clinical Software - Phoenix, AZ

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.

This position supports the development and enhancement of clinical software applications by gathering requirements, documenting workflows, and coordinating across R&D, Quality, and business stakeholders. The role will contribute to product design discussions and ensure features align with user needs and compliance requirements. The Product Analyst - Clinical Software plays a key role in translating clinical and technical expertise into actionable development tasks and supporting multiple software products.

• Support feature and enhancement prioritization by gathering requirements and documenting user needs.
• Assist with prototyping and documenting new product features or changes.
• Collaborate with stakeholders to track product requirements and ensure alignment with business needs.
• Partner with development teams to support story building, sprint planning, and product demos.
• Coordinate with Software Quality Assurance teams to review test cases and validate product readiness.
• Help monitor project timelines, follow up on action items, and report on progress.
• Support compliance and regulatory documentation related to product development.

• 3+ years of experience in software quality assurance, clinical applications, or related field.
• Familiarity with software development lifecycle (SDLC) and/or product development processes.
• Strong communication, analytical, and organizational skills.
• Ability to document requirements and translate technical details into clear workflows.
• Proficient in Microsoft Office Suite; familiarity with prototyping or visualization tools a plus.

• All job specific, safety, and compliance training are assigned based on the job functions associated with this position.

• Occasional work on evenings and weekends.
• Occasional travel is optional.

Individual must successfully complete pre‑employment process, which includes criminal background check, drug screening, credit check (applicable for certain positions), and reference verification. This job description reflects management’s assignment of essential functions. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Mid‑Senior level

Full‑time

Research, Analyst, and Information Technology