Director, Vault eTMF

Join one of the fastest growing companies in high tech! Veeva was named among the top fastest growing public technology companies on Forbes’ annual Fast Tech 25 list.  We build innovative SaaS solutions that include CRM, content management, and customer master data management for life sciences customers.

Follow us on Instagram @veevasystems or Twitter @VeevaCareers and @Veeva_EU and read the buzz, see our videos, and hear from our team about the innovation, people, and #lifeatveeva. Are you ready to innovate, inspire, and shape the future of the industry cloud? Make your best career move here!

Job Summary:

The Director, Vault eTMF EU is a critical position requiring a deep understanding of the global life sciences eTMF and clinical space. This role will be responsible for growing Veeva’s eTMF market in Europe.
In this role, you will have the opportunity to work with a team of Life Sciences industry and technology A-players, who, together, are bringing the next generation of regulated content management capabilities to the life sciences industry.

The ideal candidate will be based in UK, Belgium, Switzerland or Germany.


  • Providing thought leadership and sales support to teams in the field
  • Assisting with the development of product strategy and messaging
  • Coordinating resources across the customer lifecycle from sales to delivery and beyond
  • Presenting at industry conferences, leading webinars and authoring articles for industry publications


  • Direct experience with Trial Master File (TMF) processes; such as study start up, as a consultant or team member at a Clinical Research Organization (CRO) or sponsor, preferably across multiple life sciences organizations.
  • Significant experience working within the Clinical Operations area of life sciences sponsor or CRO and with Clinical technologies, such as eTMF, CTMS, EDC, investigator portals, site secure document exchange ,etc.
  • Proven ability to innovate across business processes or solutions.
  • Willingness to travel.
  • Fluent in English

Nice to Have:

  • Experience working for a Clinical Research Organization (CRO).
  • Experience with content management technologies.
  • Proven track record of thought leadership through industry presentations, publications or other mechanisms.
  • Strong understanding of study and site management and overall trial planning and execution.
  • Experience with selling software or services to life sciences organizations

Back to top