Director Product Management - Veeva RIM

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. In this role, you will lead a team of Product Managers working on Veeva RIM, defining product strategy and collaborating with engineering to enhance regulatory process efficiency.

Responsibilities:

• Lead and mentor a team of talented Product Managers
• Define direction on product features and vision
• Design innovative product features to support the management and submission of content that ultimately is submitted to Health Authorities worldwide
• Review and author high quality design specifications within an agile methodology
• Prioritize features based on strategic initiatives, customer requirements, and internal technical needs
• Collaborate with customers, services, support, market strategy, and sales to understand business needs and ensure customer success
• Partner with the engineering and QA teams to drive high quality product feature implementation
• Be the product evangelist - become a subject matter expert for internal stakeholders and external customers

Requirements:

• Experience leading and developing product management teams
• 3+ years in product management leadership role
• 5+ years of experience in SaaS product lifecycle and ability to develop short- and long-term product roadmap and plans based on client and market requirements
• Experience interacting with customers, development, and consulting teams, both local and remote
• Ability to work independently in a dynamic environment, with little direct supervision
• Strong communication skills: written, verbal, and formal presentation
• Technical skills to translate business requirements into terms that developers can understand
• Must be able to travel 25%
• Experience using Veeva Vault RIM
• 5+ years of experience in Regulatory (or other regulated industry)
• Working knowledge of submission publishing, review and archiving processes and procedures, understanding of various submission standards and the impact of these standards on day-to-day regulatory activities