IRT, eConsent, and eCOA solutions to help you wisely guide novel science through complex clinical trials
Clinical trial management • Interactive response technology • Subject randomization • Trial supply management • IWRS
August 22
🏡 Remote – New York
IRT, eConsent, and eCOA solutions to help you wisely guide novel science through complex clinical trials
Clinical trial management • Interactive response technology • Subject randomization • Trial supply management • IWRS
• 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 • 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 • Can serve as ‘Lead Project Tester’ on a project and have additional responsibilities: • Coordinate and monitor all testing tasks on a new study build or change control • Oversee days to day project tasks of software testing team members assigned to the project • Serve as main point of contact for all testing-related requests and questions on a project • Ensure on-time delivery of assigned new study builds with a focus on quality and risk management
• Bachelor’s degree preferred • High-achieving, exploratory nature • Attention to detail • Analytical reasoning skills • Desire to learn and grow • Strong work ethic • Sense of ownership and pro-activity • Effective prioritization and time management • Follow-through • Communication skills • eClinical domain knowledge preferred • Technical Knowledge (SQL, programming, test automation)
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