Senior Implementation Consultant - RIMS Remote

Veeva Systems is a missiondriven organization and pioneer in industry cloud helping life sciences companies bring therapies to patients faster. As one of the fastestgrowing 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. Were 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

We are looking for an experienced consultant with deep expertise in navigating customers through complex software implementation. Veevas Vault RIM suite is the industrys 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 cloudbased platform.

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

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 cloudbased 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 Youll Do

• Lead software implementation projects at life sciences companies ranging from the worlds largest pharmaceutical companies to emerging biotechs
• Lead the solution design for implementation and use of the Vault Regulatory suite (Veeva Registrations Veeva Submissions Veeva Submissions Archive Veeva Publishing)
• Lead configuration requirements workshops design prototype configure and document content solutions
• Program and project management including resource planning leading and motivating a crossfunctional team
• Primary customer liaison managing communication between the project team customer and internal stakeholders
• Mentor project team and consultants helping others improve their consulting skills

Requirements

• 8 years experience working with life sciences or healthcare companies performing system implementation experience either as a consultant business or IT representative
• Indepth knowledge of drug development processes and regulatory submissions; including Labeling Submission Publishing and / or Viewing systems
• Proven ability to collaborate and communicate excellently with diverse stakeholders and ensure delivery to a high degree of satisfaction
• Influential; experience leading teams through hard decisions and negotiating compromises
• Technical abilities and willingness to roll up your sleeves to design and implement a RIM solution
• Expert on life sciences compliance and computer systems validation requirements
• Ability to work independently in a fastpaced environment
• Ability to travel as required by the business

Nice to Have

• 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
• 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

LIRemote

Veevas headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.

As an equal opportunity employer Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender race ethnicity religion politics sexual orientation age disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.

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 .

Required Experience :

Senior IC

Key Skills