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    Dynamics Implementation Consultant - London, United Kingdom - Veeva Systems, Inc.

    Veeva Systems, Inc.
    Veeva Systems, Inc. London, United Kingdom

    1 week ago

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    Description

    Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster.

    Do the Right Thing, Customer Success, Employee Success, and Speed.

    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.

    Come help us transform how regulatory information is managed in Life SciencesVeeva'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.

    Veeva Systems is looking for leaders in Life Sciences consulting with system implementation experience and a passion for helping customers optimize their regulatory data and document management process.

    As a key member of our Professional Services team, the Senior Consultant will be responsible for understanding our customers' global regulatory needs, translating requirements into solution design, and defining global strategies for deploying 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.

    Lead software implementation projects at life sciences companies ranging from the world's largest pharmaceutical companies to emerging biotech
    Lead the solution design for how your customer will implement and use the Vault Regulatory suite (Vault Registrations, Vault Submissions, Vault Submissions Archive, Vault Publishing)
    Lead requirements workshops, design, prototype, configure and document content management/registration data solutions
    Architect multi-year and multi-phased implementation programs to deploy Vault RIM across an organization globally
    Program and project management including resource planning, leading and motivating a cross-functional team, and project tracking and forecasting
    Primary customer liaison managing communication between the project team, customer and internal stakeholders
    Mentor project team and junior consultants in the R&D Services organization
    8+ years' experience in implementing, supporting, or administering core business and IT operations related to technology solution(s),
    ~ In-depth knowledge of drug development processes and regulatory information management or regulatory submissions; Ability to travel up to 50%

    Direct experience with systems such as Veeva Vault, PAREXEL/ LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, CARA, Salesforce, Workday, Oracle, SAP, Lorenz Docubridge, Extedo eCTD Manager, Master Control, Trackwise, other regulatory information management or submission publishing systems, etc.

    Consulting experience, working with a major system integrator or software vendor
    Regulatory Affairs, Regulatory Operations or Pharmacovigilance background
    Knowledge of Pharmaceutical, Biotechnology, and/or Medical Device and Diagnostics regulatory processes, data and content
    PMP certification
    Execution experience with Agile methodology and/or ACP Certification
    Life Science, computer science or related degree
    Fluency in one or more of the following languages: German, French, Spanish, Italian
    #As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at .
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