Senior Inhouse Veeva Consultant (f/m/d)

Design. Progress. Together.


CureVac Corporate Services GmbH, a wholly owned subsidiary of CureVac SE, combines the central functions of the CureVac business group. CureVac is a global biopharmaceutical company in the field of mRNA technology, with more than 20 years of expertise in researching, developing and optimizing the versatile biological molecule for medical purposes. Our focus is on prophylactic vaccines, innovative cancer immunotherapies, and protein-based therapies. All RNA people are striving to achieve our main joint goal: To bring multiple best-in-class mRNA medicines to market.


The Digital Strategy & Governance function is responsible to define and drive CureVac’s ambitious Digital Transformation Agenda.  As a Senior Inhouse Veeva Consultant (f/m/d) at CureVac you will participate in project delivery and service management. Thereby, you drive together with our IT Veeva Team the further development and integration of our Veeva Platform. We are looking for a technical versatile profile with strong business acumen and the will to collaborate on a personal level with our team in Amsterdam, Tübingen (near Stuttgart) or Wiesbaden as


Senior Inhouse Veeva Consultant (f/m/d)



Your Responsibilities:

  • The entire life cycle of selected applications on the Veeva platform

  • Design and drive our continuous improvement and integration of our entire Veeva platform

  • Contribute to delivery projects as part of our continuous extension of our Veeva platform

  • Lead workshops, translate and implement business requirements into suitable technical solutions

  • Lead the change and release management of Veeva Systems

  • The application management of Veeva Systems including troubleshooting, issue management, configuration management and documentation

  • Manage and facilitate our vibrant key user community through workshops, trainings and knowledge exchange



Your Qualifications:


  • Master's degree in Computer Science, Information Systems or equivalent

  • Several years of relevant practical experience including but not limited to: implementing computer systems in regulated biotech or pharmaceutical companies

  • Vast experience in regulated environments (GxP)

  • Experience in 21 CFR Part 11, GAMP, project delivery, as well as working in a highly regulated environment within the pharmaceutical industry

  • Practice in the implementation of Veeva Systems

  • Capability to translate business requirements into technical specifications

  • Understanding and knowledge of IT service management (ITSM)

  • Ability to adapt to a fast-changing environment

  • Effective communication with all levels within the organization

  • Strong communication skills, a collaborative working style and analytical skills are describing your profile


We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding.
With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us.

Design your future with us – become part of the RNA people!   

We look forward to receiving your application via our CareerPortal.


CureVac Corporate Services GmbH


Human Resources
Christina Glass 
Friedrich-Miescher-Straße 15
72076 Tübingen