B.S. degree or equivalent experience with 5+ years in regulatory operations, technology, or business analysis.
Proven experience with Veeva Vault RIM, including configuration and understanding of the data model.
Knowledge of regulatory data standards such as IDMP/PMS and their relevant applications.
Experience with integrations within the Veeva ecosystem, specifically RIM and Quality systems.
Hands-on skills in gathering and documenting requirements for system enhancements.
Experience with UAT coordination and supporting validation processes.
Ability to create user documentation and training materials to facilitate system adoption.
Responsibilities
Remediate data within the Veeva RIM framework.
Spend 65-70% of time focused on Veeva RIM tasks.
Elicit, document, and translate business requirements into system enhancements for Veeva Vault RIM.
Serve as a functional subject matter expert (SME) on Veeva Vault RIM data models and regulatory structures.
Support design and optimization of Veeva Vault RIM, including necessary integrations with other Veeva systems.
Develop and maintain reports and dashboards for KPI tracking and data monitoring.
Collaborate with cross-functional teams to prioritize enhancements and optimize processes.
Benefits
Opportunity to work at the forefront of regulatory technology advancements.
Exposure to innovative AI and automation projects within regulatory processes.
Collaboration with diverse teams across regulatory functions and IT.
Chance to participate in the design and enhancement of critical regulatory systems.
Full Job Description
Roles & Responsibilities:
Looking for someone with technical experience with Veeva RIM.
This person will be remediating data.
Great to have - IDMP, eCTD, Veeva capabilities.
SDLC.
Experience with AI & the automation process space.
Experience with integration between Veeva quality to Veeva RIM.
Understands Veeva RIM reporting & KPIs.
This person will be spending 65-70% of their time in Veeva RIM.
Elicit, document, and translate business requirements into system enhancements for Veeva Vault RIM, and other systems, working closely with regulatory stakeholders, superusers, and IT teams.
Serve as a functional SME for Veeva Vault RIM, with strong understanding of the data model, including registration objects and core regulatory data structures.
Support design, enhancement, and ongoing optimization of Veeva Vault RIM, including integrations with Veeva Quality, Clinical, and PromoMats.
pply working knowledge of IDMP data models (including PMS) to support data remediation efforts and ensure accurate representation of regulatory data within Vault RIM.
Configure and support key RIM capabilities, including Global Content Plans, Active Dossier setup, and dossier management across Modules 2-5.
Partner with technical teams to support system design, validation, data migration, data cleansing, and UAT activities, including test script review.
Develop and maintain reports and dashboards across Vault RIM objects to enable KPI tracking, data monitoring, and informed business decision-making.
Collaborate cross-functionally to prioritize enhancements, drive process optimization, and ensure alignment between business needs and system capabilities.
Support user education and change management, including development of training materials, business guidelines, and reference documentation.
Communicate effectively with stakeholders at all levels; work independently and proactively to drive initiatives forward.
Contribute to broader regulatory technology strategy, including adoption of modernization approaches (e.g., AI-enabled authoring tools, labeling/CMC modernization, ICH M4Q(R2), FHIR-based standards).
Support capabilities related to eCTD submissions, including experience with or exposure to eCTD 4.0 within Vault RIM environments (preferred).
Requirements:
B.S. degree (or equivalent experience) with 5+ years of experience in regulatory operations, regulatory technology, or business analysis.
Proven experience with Veeva Vault RIM including configuration, data model understanding, and business process support.
Experience with regulatory data standards (e.g., IDMP/PMS) and their application in system implementations or data remediation efforts.
Experience with system integrations within the Veeva ecosystem (e.g., RIM-Quality).
Hands-on experience with requirements gathering, documentation, and translation into system enhancements.
Experience supporting validation processes, including UAT coordination, test script review.
Experience creating training materials, SOPs, and user documentation, and supporting adoption of new capabilities post-go-live.
Experience with reporting and analytics within enterprise systems to support KPIs and operational metrics.
Familiarity with eCTD publishing solutions; exposure to eCTD 4.0 is a plus.
Exposure to AI/GenAI tools, automation, or digital transformation initiatives in regulatory or content processes is a plus.
