Description
Veeva Systems is seeking a Computer Software Validation (CSV) professional specializing in clinical trial software, particularly Randomization and Trial Supply Management (RTSM). The role supports RTSM implementations by collaborating with development and project management teams, gathering requirements, ensuring risk-based testing, developing validation deliverables, managing testing cycles and issues, maintaining change control, and providing expertise in computer system validation and applicable regulations. The position requires knowledge of the software development cycle, strong attention to detail, and clear English communication; familiarity with GCP guidance such as 21 CFR Part 11 and EU Annex 11 is a plus.
