Veeva Systems
1001 - 5000 employees
☁️ SaaS
⚕️ Healthcare Insurance
💊 Pharmaceuticals
SaaS • Healthcare Insurance • Pharmaceuticals
Veeva Systems is a cloud-computing company focused on the global life sciences industry. It provides software, data, and consulting services to streamline research and development, quality management, regulatory operations, and commercial processes. Veeva's solutions encompass clinical trials, regulatory submissions, drug safety management, and commercial execution to support life sciences enterprises in their mission to improve and extend life.
Manager Strategy – Regulatory, LatAm
🕒 February 25
🗣️🇪🇸 Spanish Required
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Veeva Systems
1001 - 5000 employees
☁️ SaaS
⚕️ Healthcare Insurance
💊 Pharmaceuticals
SaaS • Healthcare Insurance • Pharmaceuticals
Veeva Systems is a cloud-computing company focused on the global life sciences industry. It provides software, data, and consulting services to streamline research and development, quality management, regulatory operations, and commercial processes. Veeva's solutions encompass clinical trials, regulatory submissions, drug safety management, and commercial execution to support life sciences enterprises in their mission to improve and extend life.
📋 Description
• Responsible for growing and sustaining the Regulatory market in Latam, with a primary focus in Brazil and Mexico, for the Vault RIM applications including Vault Registrations, Submissions, Submissions Archive, and Submissions Publishing (eCTD 4.0) • Provide thought leadership and sales support to teams in driving new opportunities in the Regulatory space • Develop strategy and messaging for customer adoption of new products and features, and functionality for new and existing customer base • Present at industry conferences, leading webinars, and authoring articles for industry publications • Provide business guidance to the product team in support of new or enhanced features and functionality in regulatory applications
🎯 Requirements
• 5+ years of experience with regulatory submission document authoring, submission publishing/validation/viewing, registration and commitment tracking, and regulatory document archiving • Proven ability to innovate across business processes and technology solutions • Ability to hold strategic conversations with heads of regulatory and IT regarding the regulatory applications and their use within Regulatory execution • Understanding of drug development & regulatory process in Brazil and Latam • Ability to travel for customer meetings and presentations • Fluent/Advanced in English and Spanish.
🏖️ Benefits
• Medical, dental, and life insurance • Flexible PTO and company paid holidays • 1% charitable giving program
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