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Consultant - CDMS Post-Implementation Services (Remote)

Veeva Systems
Work Anywhere - Poland
Start date
18 Oct 2021
Closing date
17 Nov 2021

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Clinical Research, Clinical Trials Manager / Administrator, Information Technology, Database Development, EDC, IT Architecture
Full Time
Contract Type
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Job Details

The Role

Veeva Systems is looking for Consultants, who wish to become experts with the Veeva Vault CDMS Portfolio, a passion for helping customers achieve their business vision, and wish to participate in the transformation of the Life Sciences industry.  

Consultants are members of our Services Organization providing post-implementation consulting as subject matter experts of Veeva Applications. 

This role is primarily a remote position working off-site with multiple clients within the EMEA region, occasionally on-site consulting activities will occur. Qualified candidates will be located in Poland.

What You'll Do

  • Clinical data management solution design, configuration, and documentation
  • Provide post-go-live System Consulting and Administration
  • Analyse and deploy new product features
  • Maintain Production and Sandbox environments
  • Execute Customer Change Requests
  • Execute configuration troubleshooting
  • Knowledge transfer and ad-hoc training of customer employees
  • Interact with Veeva Product Support on customer’s behalf
  • Support the Customer in maintaining a validated state for their Vault


  • Strong desire to learn new things
  • At least a Bachelor’s degree in Management Information Systems, Computer Science, Computer Engineering, Math, Bioengineering or other similar degrees
  • Excellent verbal and written communication skills in English
  • Ability to work remotely and independently with clients
  • Experience with fulfilling customer needs and managing expectations
  • Ability to quickly understand requirements and design & articulate potential solutions
  • Experience with configuring/supporting/implementing IT systems

Nice To Have

  • Project Management experience for enterprise software implementations
  • Experience with GxP regulations and software validation process
  • Experience working with EDC clinical software, and/or trial management software in a consultant role
  • Familiarity with CDISC, ODM, and other data management industry standards
  • SaaS/Cloud experience in the delivery of clinical trials
  • Fluency in more than one European language


Veeva is a mission-driven organization that aspires to help our customers in the life sciences industry bring their products to market, faster. Our teams develop transformative cloud software, data, services and consulting to make our customers more efficient and effective in everything they do. Founded in 2007, Veeva works with 950+ customers, operates across 165+ countries and has 4700+ employees globally. 

Our core values — do the right thing, customer success, employee success, and speed — guide our decision making and define our culture. Doing the right thing means that we are concerned about more than just financial success. Veeva became a Public Benefit Corporation in February 2021, recognising our responsibility to customers, employees and the community, in addition to shareholders' interests.  

Veeva is a Work Anywhere company, meaning you can work at home, at a customer site, or in an office on any given day. Opportunities are available across Europe - our offices are based in Oxford, Frankfurt, Paris, Barcelona and Hungary. 

Find Us
Spires House
John Smith Drive
Oxford Business Park South
United Kingdom
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