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Veeva Systems

Builds cloud software for life sciences

Senior Product Manager - Clinical Operations

Product ManagementConfirmed live in the last 24 hours
Full-timeBoston, MA, USA

About the Job

Requirements

  • At least 5 years of Product Management experience, preferably focused on B2B enterprise SaaS applications.
  • A proven track record of managing all stages of the product lifecycle and successfully launching products or features that meet customer needs.
  • Experience working in an agile development environment and collaborating effectively with engineering, quality assurance, and design teams.
  • Ability to articulate a clear vision and influence cross-functional teams without formal authority.
  • Strong analytical and problem-solving skills, with the ability to make data-informed decisions.
  • Commitment to professional integrity and ethical decision-making.
  • Ability to travel approximately 10–15% for on-site customer meetings, user research, and events.

Responsibilities

  • Own the end-to-end product lifecycle, from ideation and strategy through development, launch, and iteration for applications within the Vault Clinical Operations suite.
  • Engage with customers, industry experts, and internal stakeholders to identify market needs, gather requirements, and define a product vision.
  • Author feature specifications, user stories, and acceptance criteria in collaboration with engineering, quality assurance, and design teams.
  • Prioritize the product backlog, balancing customer enhancement requests, new features, and strategic initiatives to deliver value.
  • Serve as the subject matter expert and product evangelist for the application, communicating its vision, roadmap, and features to internal and external audiences.
  • Educate Sales, Solution Consultants, Professional Services, and Support Teams through written materials and demonstrations to drive customer adoption and support customer issues.
  • Define and analyze key metrics to measure product success, inform data-driven decisions, and demonstrate business impact.
  • Stay current with regulatory changes affecting the clinical operations domain.

Desired Qualifications

  • Direct experience and deep domain knowledge in clinical trial operations, gained from working at a pharmaceutical company, biotech, contract research organization, or clinical technology provider.
  • Experience working in a regulated environment and knowledge of industry standards such as ICH GCP and FDA 21 CFR Part 11.
  • Familiarity with the Veeva Vault Platform or other Veeva applications.

About the Company

Veeva Systems

Builds cloud software for life sciences

Veeva Systems builds cloud software and data products for pharmaceutical, biotechnology and other life sciences companies. Its applications support clinical trials, regulatory submissions, quality management, drug safety and commercial teams that work with healthcare professionals. Teams use the software to organize documents, track records and coordinate regulated work across departments on Veeva's Vault platform. Veeva earns revenue from subscriptions to its software and data products, alongside implementation, consulting and other professional services. Founded in 2007, Veeva Systems is headquartered in Pleasanton, California, United States.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Pleasanton, CA
Founded
2007

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