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Job Description
Structured overview of role & requirementsAbout This Role
Lead end-to-end implementations, upgrades, and releases for Veeva Vault RIM across Submissions, Registrations, Content, and SafetyDocs.
Own solution design addressing complex regulatory business requirements ensuring platform stability and regulatory compliance in a Life Sciences regulated environment.
Act as L3 technical SME for troubleshooting, release governance, integration operations, and compliance oversight for Veeva Vault RIM applications.
Minimum Requirements
9-11 years total experience, including 6-9 years hands-on in configuring and managing Veeva Vault RIM objects, fields, lifecycles, and workflows.
7+ years experience specifically with Veeva Vault RIM (Submissions, Registrations, Content, SafetyDocs).
Experience in GxP validated systems, CSV/CSA methodology, and ITIL-driven Incident, Problem, and Change Management processes.
Veeva Vault Certification(s) in Admin or RIM preferred.
Ideal Candidate Profile
Deep expertise in Veeva Vault RIM with ability to lead complex platform implementations and resolve L3 level issues.
Strong understanding of global regulatory processes (FDA, EMA, other Health Authorities) and compliance in Life Sciences.
Proven experience managing release & change governance, root cause analysis, and building advanced Vault reports and dashboards.