Senior Product Manager - EDC

The Role Interested in working in a fast‑paced environment that also offers the stability of a successful public company? Do you want each day of work to help bring medical products to market that save lives and improve quality of life? The Veeva EDC team may be the right fit for you. Our product helps accelerate the delivery of lifesaving drugs by transforming clinical trial processes. We’re seeking a high‑energy, passionate product manager with experience in B2B enterprise SaaS who can create a game‑changing health‑tech application that continues Veeva’s leadership in cloud‑based life‑sciences 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 a 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. Qualifications 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 such as Python, Java, SQL, etc. Familiarity with the Veeva Vault Platform or other Veeva applications. Benefits Medical, dental, vision, and basic life insurance. Flexible PTO and company‑paid holidays. Retirement programs. 1% charitable giving program. Compensation Base pay: $120,000 – $200,000. The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Actual salaries may vary within or outside the range based on experience and location. This position may also be eligible for variable bonus and/or stock bonus. 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 View email address on click.appcast.io. #J-18808-Ljbffr Veeva