Veeva Systems

Senior Consultant, MedTech RIM

Veeva Systems

full-time

Posted on:

Origin:  • 🇺🇸 United States

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Salary

💰 $80,000 - $200,000 per year

Job Level

Senior

Tech Stack

CloudVault

About the role

  • Lead MedTech customers through their regulatory transformation via implementation of Veeva RIM applications
  • Partner with customer SMEs and business leaders to analyze, develop, and implement regulatory processes supporting Veeva RIM (Submissions, Submissions Archive, Registrations, and Publishing)
  • Analyze and document current state business processes, identifying pain points and system functionality gaps
  • Define roll-out strategies for deployment of Veeva RIM across global regulatory teams
  • Serve as the primary customer liaison managing communication between project team, customer, and internal stakeholders
  • Represent Professional Services across multiple engagements and workstreams (solution design and configuration, data migration, systems integration, etc.)
  • Mentor project team and junior consultants in the Professional Services organization

Requirements

  • 8+ years of experience implementing regulatory information management systems and processes (e.g., Registration Data Tracking Systems, Submission systems)
  • Working knowledge of life sciences compliance, regulatory guidance, and day-in-the-life business processes
  • Ability to quickly understand business use cases and create process and business improvements aligned with Preferred Vault Practices
  • Experience implementing software systems, translating business requirements into solution designs
  • Proven expertise in customer leadership and mentoring of team members
  • Demonstrated stakeholder management, critical thinking, and technical communication skills across varied audiences
  • Ability to travel up to 50%
  • Opportunities available within the United States; qualified U.S.-based candidates are encouraged to apply
  • Nice to have: Direct experience with Veeva Vault, PARAXEL/LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, IQVIA, Trackwise, or other RIM systems
  • Nice to have: Consulting experience with a major software vendor or process management consulting group
  • Nice to have: Regulatory Affairs, Regulatory Operations, or Submissions Management background
  • Nice to have: Life science, computer science, biochemical or mechanical engineering or related degree
  • Nice to have: SaaS/Cloud experience