2 days ago
Remote, Romania +2 moreMid Level
Responsibilities
- Ensure the correct functioning of clinical trial software with emphasis on patient safety and clinical study data integrity.
- Verify that requirements are clear, testable, consistent, and aligned with clinical trial protocols.
- Develop validation plans using a risk-based testing methodology.
- Author and manage validation-related deliverables for projects.
- Author and execute test scripts.
- Document defects and track their resolution.
- Coordinate and monitor testing tasks when serving as Lead Project Tester.
- Oversee day-to-day testing tasks for assigned software testing team members.
- Serve as the main contact for project testing questions and requests.
- Ensure timely delivery of new study builds with a focus on quality and risk management.
Requirements
- At least 3 years of relevant experience in a similar role, including web testing on software solutions.
- Strong understanding of testing methodologies and principles.
- Bachelor’s degree preferred.
- eClinical domain knowledge preferred.
- Technical knowledge of SQL, programming, and automation preferred.
- Strong analytical reasoning, attention to detail, prioritization, communication, ownership, and follow-through skills.
About Suvoda
Suvoda builds clinical trial software for pharmaceutical and biotech sponsors and research sites, offering IRT/RTSM for subject randomization and drug supply, plus eConsent, eCOA, and integrated patient payments and travel from its merger with Greenphire. Privately held and founded in 2013, the company is headquartered in Conshohocken, Pennsylvania. It specializes in complex studies in oncology, central nervous system disorders, and rare diseases.