Senior Professional Services Consultant

7 hours ago


Copenhagen, Copenhagen, Denmark Veeva Systems Full time
Job Description
As a Senior Consultant on our Clinical Data Management System (CDMS) Professional Services team, you will be at the forefront of our mission to transform the life sciences industry. You will act as the customer's trusted advisor to ensure that the study trial design is configured in such a way that it meets their goals and offers the full benefits of Veeva's CDMS application.

This is a Work Anywhere position - you can choose to work remotely in the EU, or in one of our EU offices. Veeva Systems does not anticipate providing sponsorship for employment visa status for this position.

Key Responsibilities:
- Lead requirements-gathering sessions to understand customers' data management needs and challenges.
- Offer guidance and direction to ensure that the clinical trial is designed with the deliverable in view.
- Understand our customers' clinical trial protocol requirements, create specifications, and implement a study design with the Vault CDMS application.

Required Skills and Qualifications:
- 5+ years experience in end-to-end data management-related activities in EDC.
- Experience in interpreting clinical protocols and translating requirements into software specifications.
- Strong understanding of data management standards and guidelines (GCDMP, CDISC, SDTMIG, CDASH).


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