Team: Professional Services
City: Barcelona
Country: Spain
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 RoleTired of trying to make old technology work in pharma? Want to work for the leading cloud software provider for Life Sciences? Looking for an opportunity to do something new, exciting and with a clear value proposition for pharma and biotech customers?
Veeva is looking for an EU-based experienced R&D IT program leader to manage implementation programs at Veeva's largest Vault customers globally and guide the transformation of their R&D technology landscape. You will work closely with Veeva's Account Management Team to ensure delivery success across your Vault R&D program(s), continuous improvement of existing applications and overall Customer Success for the programs.
This role is ideal for a self-starter who works well in a remote setting and is able to travel upon business requirements. Work location is flexible, ideally close to a major EU airport. Qualified candidates must be legally authorized to be employed in the European Union or UK. Veeva Systems does not anticipate providing sponsorship for employment visa status for this employment position.
What You'll DoService Delivery accountability for one or more Global Vault implementations in Clinical, Safety, Regulatory, or Quality & Manufacturing at our strategic accountsWork with IT and business executives to define deployment, governance, and transformation roadmapSupport implementation proposals and services contract negotiationCoordinate Customer Success Manager activities to drive product value and adoptionCoordinate Product Management and Product Support activitiesRequirements7+ years in large-scale program management within the Pharmaceutical R&D space (Clinical, RIM, Quality & Manufacturing)In-depth Pharmaceutical R&D knowledge in at least 1 of the following functional areas – Clinical, Regulatory, Quality, ManufacturingTrack record of success leading diverse global teams to deliver large, complex GxP technology implementations with outstanding resultsExperience in technology strategy and roadmap development for large customers, ideally in GxP environmentsExpert in written communications and proven executive communication skillsAbility to critically and objectively interpret and evaluate information to effectively influence at the executive levelStrong knowledge of 21 CFR Part 11 requirements and Computer Systems ValidationSkills in problem resolution, negotiation, dealing with ambiguity, establishment of effective processes, influencing without authorityNice to HaveAdvanced (certified) project management skills (PMP, PMI PgMP certification)Software as a Service implementation experienceVeeva'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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