Implementation Consultant RIM

Veeva Systems, Inc.; Barcelona; A distancia; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

An innovative company is seeking experienced leaders to join their Professional Services team. This role involves implementing and designing solutions using the Veeva Regulatory suite, aimed at optimizing regulatory data and document management for life sciences customers. You will engage with diverse stakeholders, manage projects, and configure cloud-based solutions tailored to client needs. With a commitment to flexibility, this remote position allows you to thrive in your ideal work environment while making a positive impact on the industry. If you are passionate about regulatory affairs and enjoy collaborating with teams, this opportunity is perfect for you.

Formación

• 2+ years of experience in consulting or IT roles.
• Strong technical skills to implement RIM solutions.

Responsabilidades

• Implement Veeva Regulatory suite solutions for life sciences clients.
• Lead project management and configuration workshops.

Conocimientos

Consulting

Project Management

Communication

Teamwork

Technical Implementation

Educación

Bachelor's Degree

Herramientas

Veeva Vault RIM

Regulatory Information Management Software

Descripción del empleo

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 $2B 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 apublic benefit corporation(PBC), legally bound to balancing the interests of customers, employees, society, and investors.

As aWork Anywherecompany, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.

Join us intransforming 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 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

• 2+ years experience either as a consultant, business, or IT representative
• Technical abilities and willingness to “roll up your sleeves” to design 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