Posted 16 months ago

Implementation Consultant RIM

BarcelonaRemoteFull-time

AI Summary

This role implements Veeva Vault RIM solutions for life sciences customers, configures cloud-based regulatory information management workflows, and leads workshops and projects.

About this role

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.

At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.

As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.

Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

The Role

Veeva Systems is looking for individual leaders with consulting and system implementation experience and a passion for helping customers optimize their regulatory data and document management processes.

Veeva’s Vault RIM suite is the industry’s only unified software solution that provides fully integrated regulatory information management (RIM) capabilities, including data and document management, submission publishing, and archival on a single cloud-based platform.

As a member of our Professional Services team, you will be responsible for understanding our customers’ global regulatory needs, translating requirements into solution design, and configuring our cloud-based solution for managing regulatory information across the enterprise.

There is no work location requirement (remote position) within the EU/UK if a candidate is in close proximity to an airport and able to meet travel requirements. Qualified EU/UK-based candidates are encouraged to apply.

What You'll Do

Implement software and design solutions with our Veeva Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Submissions Publishing) at life sciences customers

Lead configuration requirements workshops, design, and document, as well as prototype and deploy solutions

Program and project management, including resource planning, leading and motivating a cross-functional team

Communicate between the project team, customer, and internal stakeholders

Requirements

3+ years in technology implementation services, in life sciences or healthcare

Technical abilities and willingness to “roll up your sleeves” to design, configure and implement a RIM solution

Ability to collaborate and communicate excellently with diverse stakeholders

Team player with strong organization skills and an ability to work hard in a fast-paced environment

Ability to travel as required by the business

Nice to Have

Consulting experience, working with a major system integrator or software vendor

Knowledge of drug development, Regulatory Affairs, or Regulatory Operations

Experience in life sciences compliance and computer systems validation requirements

Fluency in one or more of the following languages: English, German, French, Spanish, Italian

Skills

Cloud-based PlatformsComputer Systems ValidationConfigurationData And Document ManagementEnglishFrenchGermanItalianLife Sciences ComplianceProgram And Project ManagementPrototype DevelopmentRegulatory Information Management (RIM)Resource PlanningSpanishStakeholder CommunicationSubmission PublishingTravel WillingnessVeeva RegistrationsVeeva Regulatory SuiteVeeva SubmissionsVeeva Submissions ArchiveVeeva Submissions PublishingWorkshops