Veeva Systems

Compensation

Full Description

Job Description: • Responsible for growing and sustaining the MedTech market for Vault applications, including Submissions, Registrations, Submission Publishing, and others as determined in the future • Provide thought leadership and sales support to teams in driving new opportunities in the Regulatory space • Provide business and technology guidance to the Product team in support of new or enhanced features and functionality in defined applications • Develop strategy and messaging for customer adoption of new features and functionality for a new and existing customer base • Coordinate resources across the customer lifecycle from sales to delivery and beyond • Present at industry conferences, lead webinars, and author articles for industry publications Requirements: • Direct experience and understanding of global regulations for medical devices and diagnostics • Hands-on experience in one or more of the following areas: Regulatory Affairs/Regulatory Operations tasks, including submissions for US, EU, and ROW • 5+ years of experience working within the medical device and diagnostics space through a manufacturer, technology solution provider, or partner • Proven ability to innovate across business processes and technology solutions in the context of business transformations • Ability to hold meaningful conversations with heads of Regulatory Affairs and IT regarding content and data application use across an organization • Ability to travel for customer meetings and presentations • Proven and direct experience in technology transformation experience, working across regulatory and IT teams Benefits: • Medical, dental, vision, and basic life insurance • Flexible PTO and company paid holidays • Retirement programs • 1% charitable giving program