Clinical Trial Software Validation Engineer II

Suvoda

United States

Remote

USD 90,000 - 120,000

Full time

14 days+

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Job summary

Suvoda in the United States seeks a tester to validate software used in complex, time-sensitive clinical trials, with a strong focus on patient safety, data integrity, regulatory alignment and dependable delivery. You will review requirements, develop risk-based validation plans, write and execute test scripts, and document results while maintaining traceability of defects.

With sufficient experience, you may lead a study build or change-control project.

Qualifications

  • At least 3 years of software testing experience, including web applications.
  • Strong understanding of testing methods and validation principles.
  • Excellent written and verbal communication skills.
  • Detail-oriented with analytical reasoning and curiosity.
  • Bachelor's degree preferred; clinical knowledge advantageous.

Responsibilities

  • Review requirements to confirm they are clear, testable, internally consistent, and aligned with the applicable clinical trial protocol.
  • Create risk-based validation plans and prepare or manage the required validation documentation.
  • Write and execute test scripts for clinical trial software and record results accurately.
  • Identify, document, prioritize, and follow defects through resolution while maintaining traceability.
  • Follow established quality processes and procedures for all testing activities and deliverables.
  • When acting as lead project tester, coordinate testing work, support assigned testers, answer testing-related questions, and help deliver study builds on schedule.

Skills

Software testing
Web testing
Analytical thinking
Attention to detail
Time management
Communication skills

Education

Bachelor's degree preferred

Tools

SQL
Programming
Test automation

Job description

Suvoda in the United States seeks a tester to validate software used in complex, time-sensitive clinical trials, with a strong focus on patient safety, data integrity, regulatory alignment and dependable delivery. You will review requirements, develop risk-based validation plans, write and execute test scripts, and document results while maintaining traceability of defects.

With sufficient experience, you may lead a study build or change-control project.

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