Senior Implementation Consultant – RIMS (Remote)

Overview

As a Senior Consultant at Veeva, you guide complex software implementations for life sciences clients using the Vault Regulatory suite. You translate regulatory needs into scalable cloud-based solutions and shape global deployment strategies. You will collaborate with cross-functional teams, mentor peers, and act as the main liaison with customers to ensure successful outcomes. This role offers the chance to influence regulatory information management at scale, within a mission-driven, flexible Work Anywhere environment.

Responsibilities

• Lead end-to-end software implementation projects for large pharma and biotech customers
• Drive solution design for Vault Regulatory suite including Registrations, Submissions, Archive, and Publishing
• Lead configuration workshops, prototyping, configuration, and documentation of content solutions
• Manage program and project activities, including resource planning and cross-functional leadership
• Serve as primary liaison between project team, customers, and internal stakeholders
• Mentor project teams and consultants to enhance consulting skills

Key requirements

• 8+ years of system implementation experience in life sciences or healthcare
• Deep knowledge of drug development processes and regulatory submissions (Labeling, Submission Publishing/Viewing)
• Proven collaboration and communication with diverse stakeholders to achieve high satisfaction
• Influential with experience guiding teams through difficult decisions and compromises
• 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
• Ability to travel as required by the business

• collaboration
• clear communication
• leadership
• Vault Regulatory suite (Registrations, Submissions, Archive, Publishing)
• RIM (Regulatory Information Management)
• data and document management

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