Senior Implementation Consultant - Rims (Remote) - Veeva Systems
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Job description
OverviewAs a Senior Consultant, you will guide complex Vault RIM implementations for global life sciences clients.You translate regulatory needs into scalable solution designs and drive deployment strategies across enterprises.You’ll lead cross-functional teams, manage stakeholders, and mentor peers to deliver high-impact regulatory information management outcomes.This role blends hands-on design with strategic delivery in a fast-growing, mission-driven SaaS environment.You will work in a flexible, work-anywhere setting with travel as needed to meet client needs.Compensaciones / BeneficiosWork Anywhereremote/hybrid/work from home optionopportunity to impact life sciencesglobal exposureflexible work locationsResponsabilidadesLead software implementation projects for pharma and biotech customersDesign and enable the Vault Regulatory suite deployment (Registrations, Submissions, Archive, Publishing)Lead configuration workshops, prototype, configure, and document content solutionsProgram and project manage, including resource planning and cross-functional team leadershipServe as primary customer liaison for project communication with stakeholdersMentor project teams and consultants to develop consulting skillsRequisitos principales8+ years of experience in system implementations for life sciences or healthcareDeep knowledge of drug development processes and regulatory submissionsStrong collaboration and communication with diverse stakeholdersInfluential leadership experience guiding teams and negotiating outcomesTechnical ability to design, configure, and implement a RIM solutionExpertise in life sciences compliance and computer systems validationAbility to work independently in a fast-paced environmentWillingness and ability to travel as requiredcollaborationclear communicationleadership/influenceVault Regulatory suite design and implementationRegulatory information management (RIM)Submission publishing and viewing systems
Requirements
Requisitos principales8+ years of experience in system implementations for life sciences or healthcare Deep knowledge of drug development processes and regulatory submissions Strong collaboration and communication with diverse stakeholders Influential leadership experience guiding teams and negotiating outcomes Technical ability to design, configure, and implement a RIM solution Expertise in life sciences compliance and computer systems validation Ability to work independently in a fast-paced environment Willingness and ability to travel as required collaboration clear communication leadership/influence Vault Regulatory suite design and implementation Regulatory information management (RIM) Submission publishing and viewing systems
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