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 lead the design and evolution of Veeva EDC products, defining features, requirements, integrations, and development plans. The role will collaborate with customers, engineering, professional services, sales, and other stakeholders to deliver innovative clinical trial technology.

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