Life Science Veeva Senior Manager

Senior Manager role in Deloitte's Life Sciences R&D team, focusing on leading client engagements, driving clinical transformation, and applying AI/ML technologies to improve drug development and business processes. Requires significant consulting and life sciences industry experience, with a focus on regulatory affairs and AI/GenAI applications.

What you'd actually do

  1. Leading engagement planning, budgeting, staffing, and delivery for complex client engagements
  2. Managing executive client and sponsor relationships and driving alignment on solutions, deliverables, and outcomes
  3. Leading clinical transformation initiatives, including operating model changes and process redesign across drug development workflows
  4. Applying technologies such as generative artificial intelligence (GenAI), artificial intelligence (AI), machine learning (ML), and automation to improve clinical and business processes
  5. Leading business development efforts, including pursuits, proposal development, pricing strategy support, and team leadership and coaching

Skills

Required

  • 8+ years of consulting experience
  • 6+ years of life sciences industry experience in pharmaceutical research and development regulatory affairs
  • 6+ years of experience leading, managing, and delivering end-to-end engagements with teams across multiple locations
  • Experience with submissions management, labeling, chemistry, manufacturing, and controls change control, lifecycle management, or submissions package development
  • Ability to travel 50%

Nice to have

  • Veeva certification
  • Experience leading proposal development and pursuit activities for consulting engagements
  • Experience leading virtual teams across multiple locations
  • Experience delivering multiple strategic engagements for large global organizations
  • Experience presenting to executive stakeholders and large and small audiences

What the JD emphasized

  • artificial intelligence/generative artificial intelligence for regulatory content generation, regulatory intelligence, or clinical trial optimization