Team: Product Management & Alliances
City: Toronto
Country: Canada
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.
Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

REQUIREMENTS

• 3+ years experience in one or more of the following industries and roles: commercial software (e.g., product management, solutions consulting, customer success), quality assurance, CMC, clinical development (e.g., clinical operations), pharmacovigilance, regulatory affairs, or regulatory operations in the life sciences industry
• Working knowledge of regulatory processes and procedures in at least one regulated sector of the life sciences industry (e.g., regulatory, clinical, commercial, quality, pharmacovigilance, CMC)
• Excellent research, analysis, and interpretation skills, with a strong ability to discern high-quality source information from low
• Excellent verbal and written communication and presentation skills, with the ability to translate complex regulatory requirements into easy-to-understand information for multiple internal teams
• Highly organized with exceptional attention to detail
• Self-starter, driven, and able to work independently as well as part of a team
• Excellent working skills with office software (e.g., MS Office, Google Suite)
• Willingness to travel occasionally to Veeva offices
• Located on the east coast of the United States or Canada

THE ROLE

We are looking for a Regulatory Intelligence Analyst to work alongside other analysts to ensure the product stays current with regulatory guidance, specifications, data standards, and requirements of global health authorities. You will identify, monitor, interpret, and communicate new or changing requirements to ensure the product stays current, and other internal teams are informed and knowledgeable of the latest regulatory intelligence. You will work directly with Product Management on compliance-related features and with other Regulatory Intelligence Analysts to continually improve our internal processes.

WHAT YOU’LL DO

• Identify regulatory requirements related to the product and implement best practices for monitoring, interpreting, and communicating changes to internal teams
• Proactively monitor, investigate, interpret, and communicate changes to regulatory requirements that may impact the current product
• Proactively monitor the global regulatory landscape for upcoming health authority initiatives or projects that may impact the product in the future
• Work directly with product management to translate regulatory requirements into Veeva’s framework for use within our suite of applications
• Translate long and complex regulatory guidance into clear, concise, and easy-to-understand information for different internal teams
• Work with a team of Regulatory Intelligence Analysts to continually improve the processes and tools used for collecting, documenting, managing, and communicating regulatory intelligence