Senior Implementation Consultant

Summary

Join Veeva Systems, a leading life sciences industry cloud company, as a Senior Consultant in Professional Services. You will lead software implementation projects for life sciences companies, designing solutions using Veeva's Vault RIM suite. This remote position (EU/UK based candidates encouraged, proximity to airport required for travel) requires expertise in regulatory information management and drug development processes. You will collaborate with diverse stakeholders, mentor team members, and ensure high-quality project delivery. Veeva offers a flexible work environment and is committed to employee success.

Requirements

• 8+ years experience working with life sciences or healthcare companies performing system implementation experience either as a consultant, business or IT representative
• In-depth 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 fast-paced environment
• Ability to travel as required by the business

Responsibilities

• Lead software implementation projects at life sciences companies ranging from the world's largest pharmaceutical companies to emerging biotechs
• Lead the solution design for implementation and use of the Vault Regulatory suite (Vault Registrations, Vault Submissions, Vault Submissions Archive, Vault Publishing)
• Lead configuration requirements workshops, design, prototype, configure, and document content solutions
• Program and project management, including resource planning, leading and motivating a cross-functional 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

Preferred Qualifications

• 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
• SaaS/Cloud experience
• Fluency in one or more of the following languages: German, French, Spanish, Italian

Benefits

Work Anywhere company, we support your flexibility to work from home or in the office