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Salary: USD 75,000 - 165,000 / annual
Veeva Systems is a public benefit corporation and pioneer in industry cloud for life sciences, with $3B+ in annual revenue. The company is seeking a Product Manager to drive core features and enhancements for the Vault Clinical Operations suite, transforming how the life sciences industry runs clinical trials.
In this role, you will execute the end-to-end product lifecycle for specific features within the Clinical Operations suite, from concept through release and iteration. You'll engage directly with customers, domain experts, and internal stakeholders to gather business requirements and understand clinical workflows. You will author clear feature specifications, user stories, and acceptance criteria for Engineering, QA, and UX design teams, and manage the product backlog by balancing customer requests, enhancements, and strategic initiatives.
You'll serve as an application expert, educating Sales, Solution Consultants, Professional Services, and Support teams through documentation and product demos. You will track key usage metrics to evaluate feature performance and inform data-driven product decisions, while staying aligned with regulatory guidelines and industry updates impacting clinical trial management. Travel up to 15% is expected for customer research and internal events.
Veeva operates as a Work Anywhere company, supporting flexibility to work from home or in the office. The company is committed to employee success, customer success, doing the right thing, and speed.
REQUIREMENTS:
- 3+ years of Product Management experience, preferably within B2B enterprise SaaS applications
- Proven track record of managing product features through the development lifecycle to successful launch
- Experience working within an agile software development environment
- Strong communication and cross-functional collaboration skills with ability to articulate clear product requirements
- Analytical mindset with strong problem-solving capabilities
- Commitment to professional integrity and ethical decision-making
- Ability to travel up to 15% for customer research and internal events
NICE TO HAVE:
- Domain knowledge in clinical operations (e.g., eTMF, CTMS, SSU, or CDMS) from pharma, biotech, CRO, or life sciences technology vendor background
- Experience in regulated industries (e.g., GCP, 21 CFR Part 11)
- Familiarity with the Veeva Vault Platform
