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Software Test Engineer II

Posted 2024-11-21

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💎 Seniority level: Middle, At least 1+ years of experience

📍 Location: Romania

🔍 Industry: Clinical trial technology

🗣️ Languages: English

⏳ Experience: At least 1+ years of experience

🪄 Skills: SQLCommunication SkillsAttention to detailTime Management

Requirements:
  • Bachelor's degree preferred.
  • At least 1+ years of experience in IRT or related field preferred (software testing).
  • English proficiency.
  • High achieving, exploratory nature.
  • Attention to detail.
  • Analytical reasoning skills.
  • Desire to learn and grow.
  • Strong work ethic.
  • Sense of ownership and proactivity.
  • Effective prioritization and time management.
  • Follow through.
  • Communication skills.
  • eClinical domain knowledge preferred.
  • Technical Knowledge preferred (SQL, programming, automation).
Responsibilities:
  • Ensure the correct functioning of clinical trial software with a focus on patient safety and integrity of clinical study data.
  • Verify that requirements are clear, testable, and consistent with the clinical trial protocol.
  • Ensure all activities and deliverables comply with Suvoda processes and procedures.
  • Develop validation plans according to a risk-based testing methodology.
  • Author and/or manage the completion of all validation-related deliverables on each project.
  • Author and execute test scripts.
  • Document defects and track resolution.
  • Perform other related duties as required.
  • Coordinate and monitor all testing tasks on a new study build or change control as a 'Lead Project Tester.'
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  • At least 1+ years of experience in IRT or related field preferred.
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  • Ensure the correct functioning of clinical trial software focusing on patient safety and data integrity.
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  • Develop validation plans per risk-based testing methodology.
  • Author and manage validation deliverables, execute test scripts, document defects, and track resolutions.
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  • Effective prioritization and time management.
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  • Ensure the correct functioning of clinical trial software with focus on patient safety and integrity of clinical study data.
  • Verify that requirements are clear, testable, and consistent with the clinical trial protocol.
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  • Develop validation plans according to a risk-based testing methodology.
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