Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.
At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.
As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.
Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.
The Role Do you consider yourself an expert in implementing or maintaining a Clinical Trial Management System? Are you excited about solving clinical trial business problems using modern CTMS technology? Do you know all about monitoring visits, recruitment plans, or site payments?
As a member of our Professional Services team, you will be responsible for understanding our customers' challenges and clinical needs, translating requirements into solution design in our Clinical Vault, delivering training, and supporting customers during application validation.
If you are a Senior Consultant, you will also be leading and mentoring talented project team members implementing and configuring the designed solution together with you.
This is a remote position. You can work from home, wherever you live in Europe. You can also work from one of our offices if you prefer to, in Paris, Oxford, Frankfurt, Budapest or Barcelona.
What You'll DoParticipate in workshops to discuss Clinical Trial Management System requirements with customersGuide customers toward the best design decisionsDocument design decisions and configure Veeva Vault or advice on Veeva Vault configuration to match customer requirementsSupport customers in validation activitiesDeliver onsite or remote trainingCollaborate with our product team on enhancement requests based on project experienceHave fun and work with an awesome team!RequirementsExperience in implementing or maintaining a CTMS solution on the vendor side, the business side, or the IT sideKnowledge of one of the following systems: IMPACT CTMS, Medidata Rave, Bioclinica CTMS, or any smaller CTMS publisher or "homegrown" solutionsProven ability to work independently in a dynamic environmentAbility to travel as requiredBachelor's degree or aboveGood communication skills in EnglishQualified candidates must be legally authorized to be employed in the European Union. Veeva Systems does not anticipate providing sponsorship for employment visa status for this employment position.Nice to HaveLife-science or computer science-related degreeExperience with Clinical Trial managementUnderstanding of technical concepts like web services or SQL queriesUnderstanding of Software Validation within life scienceSaaS/Cloud experienceExperience with Agile projectsExperience in demoing software applications in product pre-salesFluency in one or more of the following languages: German, French, Italian or SpanishPerks & BenefitsCompetitive packageAllocations for continuous learning & developmentHealth & wellness programs#RemoteSpain Veeva's headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.
If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at******.
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