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We are seeking an experienced Sr. Clinical Validation Analyst to support the development, validation, and testing of EDC systems within clinical trials. The ideal candidate will have strong expertise in Medidata Rave, demonstrated experience in peer review and UAT coordination, and a deep understanding of clinical data workflows.
Job Responsibility:
Develop, validate, and maintain study builds within Medidata Rave
Validate edit checks, custom functions, and other programmed components
Perform end‑to‑end testing of clinical study components to ensure system accuracy and compliance
Conduct detailed peer review of edit checks, custom functions, forms, and datasets
Ensure alignment with study requirements, protocol specifications, and data management plans
Facilitate and coordinate User Acceptance Testing (UAT) with cross‑functional teams
Prepare UAT documentation, track findings, and ensure all issues are resolved before go‑live
Support study teams and end users during UAT cycles
Requirements:
Minimum 5+ years of hands‑on EDC development experience within biotechnology or pharmaceutical organizations
Advanced experience with Medidata Rave, including testing of multiple study components
Bachelor’s degree in Life Sciences, Computer Science, or a related field
Nice to have:
Strong understanding of clinical data management processes
Ability to work independently and manage multiple projects simultaneously
Excellent communication, documentation, and problem‑solving skills
What we offer:
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others