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Regulatory Business Analyst

Job in Avenel, Middlesex County, New Jersey, 07001, USA
Listing for: Katalyst Healthcares & Life Sciences
Full Time position
Listed on 2026-07-18
Job specializations:
  • IT/Tech
    Data Analyst, IT Business Analyst, Business Systems & Technology Analysis
Job Description & How to Apply Below
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 Promo Mats.
  • Apply 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.
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