Key Responsibilities include:
• Gather, analyze, and document business requirements from Pharmacovigilance and Safety Document Management.
• Act as the primary liaison between business stakeholders and technical teams, ensuring requirements are clearly understood and translated into solution specifications.
• Conduct fit-gap assessments and recommend industry best practices for the respective Vault solutions.
• Prepare and/or review project and validation deliverables, including URS, FS, DS, IQ/OQ, and Traceability Matrix.
• Lead User Acceptance Testing (UAT), validation activities, and business adoption efforts.
• Support release planning, impact assessments, and change management activities.
• Provide business process expertise and guidance on platform capabilities.
Required Skills & Experience:
• Strong understanding of the relevant business processes such as Case Management and Safety Operations & Compliance Processes
• 3–8 years of experience in Life Sciences and relevant Veeva Vault Safety domain knowledge.
• Experience participating in Veeva Vault implementations, enhancements, validation, and UAT activities.
• Hands-on Veeva Vault configuration knowledge such as object models, lifecycles, workflows, security, notifications, and business rules
• Relevant Veeva Safety and Platform certifications would be an added advantage.