Veeva RIM Business Analyst & Managed Services Consultant
Job in
Scranton, Lackawanna County, Pennsylvania, 18512, USA
Listed on 2026-07-21
Listing for:
Slipstream IT, LLC
Full Time
position Listed on 2026-07-21
Job specializations:
-
IT/Tech
IT Business Analyst, Business Systems & Technology Analysis
Job Description & How to Apply Below
Veeva RIM Business Analyst & Managed Services Consultant
At Slipstream, we work to streamline IT Support and provide managed solutions with a strategic consulting and global leadership management approach. Our solutions are designed exclusively for emerging pharma and biotech organizations.
Slipstream’s industry-leading solutions free clients from the demands of internal IT and allow them to rapidly advance their mission. Led by a leadership team that has been together for over 10 years, you will join a proven team, culture, and strategy to drive innovation within the IT outsourcing industry while developing your skillset with the opportunities for internal growth.
Job SummaryThe RIM Business Analyst & Managed Services Consultant is responsible for:
- Serving as the primary liaison between Regulatory Affairs/Operations business stakeholders and IT/platform teams, translating regulatory business needs into system requirements and configuration specifications.
- Supporting implementation, migration, and ongoing managed services engagements across Regulatory Information Management (RIM) platforms, independent of underlying vendor (e.g., Veeva Vault RIM, Generis CARA, Ennov RIM, Aris Global LOOP, Master Control RIM, EXTEDO RIMS).
- Facilitating requirements gathering, process mapping, and vendor-neutral system evaluation to support client regulatory technology strategy and roadmap decisions.
- Acting as the functional point of contact for client-reported issues, enhancement requests, and release management activities, coordinating with technical configuration and IT teams to deliver resolution.
- Business Analysis & Requirements
- Facilitate requirements-gathering workshops with Regulatory Affairs/Operations stakeholders to capture business needs, pain points, and process gaps.
- Translate business requirements into functional specifications, user stories, and configuration/change requests for IT and system configuration teams.
- Conduct as‑is/to‑be process mapping for regulatory submission, registration, and publishing workflows.
- Perform vendor‑neutral system evaluations and gap assessments across RIM platforms (Veeva Vault RIM, Generis CARA, Ennov RIM, Aris Global LOOP, Master Control RIM, EXTEDO RIMS) to support platform selection and roadmap decisions.
- Serve as the primary liaison between Regulatory Affairs/Operations business owners and internal or client IT, data, and platform engineering teams.
- Own the requirements traceability matrix and ensure configuration changes reflect approved business requirements.
- Coordinate with platform administrators (Veeva Vault Admin, Salesforce Admin, or equivalent) to implement approved configuration changes across document types, life cycles, workflows, security models, and integrations.
- Define integration requirements between RIM systems and adjacent enterprise platforms (Salesforce CRM/Health Cloud, SAP, Service Now, Quality and Safety systems) where regulatory data flows across the broader enterprise landscape.
- Own intake, triage, and prioritization of managed services requests and tickets across client RIM environments, regardless of platform.
- Support release management processes, including regression testing coordination, UAT script development and execution, and release notes review, for whichever RIM or adjacent platform a client operates.
- Identify and document process improvement and automation opportunities across the regulatory technology landscape.
- Maintain SOPs, business process documentation, and system configuration specifications for client‑facing and internal use.
- Apply working knowledge of eCTD structure (ICH M8) and regional submission requirements (FDA, EMA, Health Canada) to inform requirements and configuration recommendations, independent of the publishing or RIM platform in use.
- Support Submission Content Plan design, registration/license data modeling, and health authority correspondence tracking requirements across RIM platforms.
- Develop and deliver end‑user training, quick reference guides, and change…
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