Senior Product Manager - EDC

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. The Senior Product Manager will be responsible for creating a game-changing health tech application, driving innovative product features, and managing product integrations to help continue Veeva’s success in the Life Sciences industry.

Responsibilities:

• Design and drive innovative product features based upon industry requirements across the entire Veeva EDC family of applications
• Directly responsible for designing features that will provide rich user experience while maintaining a streamlined user interaction model
• Generate wireframes, product requirements, and direct functional design
• Communicate specific, actionable requirements to members of the engineering team
• Drive customer initiatives through the development team
• Interact with Customers, Professional Services, Market Owners, and Sales to understand business needs and act as their primary development point of contact
• Manage the definition and evolution of product integrations among Veeva EDC products
• Analyze requirements, prepare technical specifications, create development and testing plans based on interaction with Senior Management
• Perform market and competitive analysis
• Demonstrate product features to internal and external audiences

Requirements:

• 5+ years of product management experience, preferably with a focus on B2B enterprise SaaS applications
• Proven track record of managing all stages of the product lifecycle and successfully launching products or features that meet customer needs
• Exceptional communication and presentation skills, with the ability to articulate a clear vision and influence cross-functional teams without formal authority
• Excellent spoken and written communication skills
• Strong analytical and problem-solving skills, with a demonstrated ability to make data-informed decisions
• Direct experience and deep domain knowledge in clinical trials, gained from working at a pharmaceutical company, biotech, CRO, or a clinical technology provider
• Experience working in a regulated environment and knowledge of industry standards such as ICH GCP and FDA 21 CFR part 11
• Undergraduate or graduate degree in computer science or engineering
• Experience with programming languages (Python, Java, SQL, …)
• Familiarity with the Veeva Vault Platform or other Veeva applications