Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.
At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a
public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.
As a
Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.
The Role
This Director role requires a deep understanding of the global life sciences Regulatory Operations space, RegOps business processes, and supporting technology solutions. This role will be responsible for growing Veeva’s Regulatory Information Management market share. In this role, the individual will have the opportunity to work with a team of Life Sciences industry and technology A-players, who, together, are bringing the next generation of Regulatory applications and capabilities to the life sciences industry.
What You'll DoResponsible for growing and sustaining the Regulatory market for the Veeva RIM applications including Vault Registrations, Submissions, Submissions Archive, and Submissions PublishingProvide thought leadership and sales support to teams in driving new opportunities in the Regulatory spaceProvide business and technology guidance to the product team in support of new or enhanced features and functionality in regulatory applicationsDevelop strategy and messaging for customer adoption of new features and functionality for new and existing customer baseSales & ConsultingCoordinate resources across the customer lifecycle from sales to delivery and beyondPresent at industry conferences, leading webinars and authoring articles for industry publicationsRequirements5+ years of experience with regulatory submission document authoring, submission publishing / validation / viewing, registration and commitment tracking, and regulatory document archiving4+ years of experience consulting for the regulatory operations area of a life sciences company3+ years of experience selling software and/or services to life sciences organizationsProven ability to innovate across business processes and technology solutionsAbility to hold strategic conversations with heads of regulatory and IT regarding the regulatory applications and their use within Regulatory executionUnderstanding of global drug development & regulatory processAbility to travel for customer meetings and presentations#LI-RemoteUS
#LI-Director
Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.
Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at
talent_accommodations@veeva.com.
