Manager, Industry Solutions, Veeva Life Science

Deloitte Deloitte · Consulting

Manager role at Deloitte focused on Life Sciences and Health Care, specifically involving Veeva Vault implementations and deploying AI/GenAI capabilities for regulatory content generation, regulatory intelligence, and clinical trial optimization. Requires consulting and Life Sciences industry experience, with a focus on Pharmaceutical R&D regulatory affairs functions.

What you'd actually do

  1. lead and deliver small engagements, or components of large, complex engagements that identify, design and implement creative business and technology solutions for our clients
  2. craft solutions for clients, guide and oversee the quality of your team’s deliverables and recommendations, as well as manage day-to-day stakeholder relationships
  3. contribute to Deloitte’s thought leadership, play a significant role in business development activities (to include, the development and presentation of proposals), and own responsibility for the development of junior staff

Skills

Required

  • 6+ years experience with relevant consulting experience
  • 4+ years of Life Sciences industry experience in the Pharmaceutical R&D regulatory affairs function
  • Veeva Vault implementations of Veeva RIM, Clinical, Quality, and/or Safety
  • Experience with deploying AI/GenAI capabilities for regulatory content generation, regulatory intelligence, clinical trial optimization
  • digital transformations / innovations
  • Understanding of Veeva data models, regulatory data structures, standards, governance and regulatory filing requirements
  • submissions management, labeling, CMC change control and/or LCM processes
  • submissions packages
  • 1+ years experience leading, managing and delivering engagements end-to-end with resources in multiple locations
  • Bachelor’s Degree

Nice to have

  • Experience leading, managing and delivering complex consulting engagements with resources in multiple locations
  • Ability to orchestrate, lead, and influence virtual teams, ensuring successful implementation of customer projects
  • Demonstrated experience with management and delivery of multiple strategic engagements for large global organization
  • Presentation skills with a high degree of comfort with both large and small audiences
  • Strong problem solving and troubleshooting skills with the ability to exercise mature judgment
  • Veeva certification strongly preferred

What the JD emphasized

  • Veeva Vault implementations of Veeva RIM, Clinical, Quality, and/or Safety
  • Experience with deploying AI/GenAI capabilities for regulatory content generation, regulatory intelligence, clinical trial optimization
  • Understanding of Veeva data models, regulatory data structures, standards, governance and regulatory filing requirements
  • submissions management, labeling, CMC change control and/or LCM processes