Software Quality Engineer (V&V)

Clario

Job Overview

Location

United States Remote

Job Type

Full-time

Full Job Description

📋 Description

• As a Software Quality Engineer (V&V) at Clario, you will play a critical role in validating clinical study software to ensure it meets the highest standards of quality, compliance, and reliability—directly supporting the delivery of life-changing therapies to patients by enabling trustworthy clinical trial data.
• You will work at the intersection of software quality and healthcare innovation, ensuring that the tools used in clinical trials are rigorously tested and validated so that researchers and sponsors can rely on accurate, auditable results that accelerate medical breakthroughs.
• Your day-to-day responsibilities will include reviewing software specifications and validation documentation to ensure clarity, completeness, and testability; designing and developing comprehensive test cases covering functional, integration, and performance scenarios; executing manual test cases, capturing detailed test evidence, and managing accurate test data for validation activities.
• You will analyze test results to identify defects, document reproducible issues with clear root cause insights, and collaborate closely with developers and project teams to validate new features while ensuring robust regression coverage across multiple projects.
• You will manage the full defect lifecycle—prioritizing, retesting, and tracking issues within bug management systems—and maintain and configure test environments, including backend systems and supporting tools, to ensure consistent and reliable testing conditions.
• You will create and maintain validation documentation aligned with SOPs, regulatory standards, and Good Clinical Practices (GCP), and support internal and external audits by preparing and providing required validation evidence.
• You will monitor project timelines, risks, and testing progress, delivering clear status updates and escalations as needed, while contributing to test planning, effort estimation, and cross-project coordination.
• You will actively identify opportunities to improve testing processes, tools, and overall quality practices, and collaborate across teams to share knowledge, support onboarding, and mentor new team members.
• Clario is a mission-driven organization dedicated to transforming lives by unlocking better evidence—your work will directly contribute to advancing clinical science and bringing innovative therapies to patients faster through reliable, compliant software solutions.
• You will join a collaborative, inclusive, and purpose-led team that values diversity, continuous learning, and innovation, where your expertise in software quality will be recognized and leveraged to elevate the standard of clinical trial technology across global studies.

🎯 Requirements

• Bachelor’s degree in Information Technology or a related field, or equivalent practical experience
• 1–3 years of experience in software testing or quality assurance
• Proven understanding of the software development lifecycle and validation processes
• Experience designing and executing manual test cases and documenting results
• Familiarity with defect tracking systems, test management tools, and documentation systems
• Basic knowledge of test automation and Agile methodologies
• Strong analytical and problem-solving skills with high attention to detail
• Effective communication skills in English, both written and verbal
• Ability to manage multiple priorities, meet deadlines, and work independently or collaboratively
• Based in or able to work remotely within the United States

🏖️ Benefits

• Competitive compensation
• Health, dental, and vision coverage
• 401(k) retirement plan with company match
• Paid time off and company holidays
• Flexible/remote work options

Skills & Technologies

GCP

Remote

Degree Required

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Clario

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About Clario

Clario is a global healthcare technology and services company that provides endpoint data solutions for clinical trials. It delivers imaging, cardiac safety, respiratory, eCOA, and precision motion technologies, supported by scientific and regulatory expertise, to help biopharmaceutical sponsors generate high-quality evidence and accelerate drug development.

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