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.
The Role
Veeva is looking for an experienced Clinical Data Programmer to support internal and customer teams in the configuration of Veeva CDB. This is a hands-on programming role that also plays a critical part in providing consultation and guidance to customers on the best practices for implementing Veeva CDB. You will work closely with the customer data management team and the Veeva CDB Project Manager to ensure successful implementation and adoption of Veeva CDB while also contributing to the evolution and improvement of Veeva CDB.
Veeva Clinical Database (CDB) is a next-generation clinical data platform that centralizes and automates data imports, cleaning, and management for clinical trials. To handle the massive expansion of trial data sources, Veeva CDB is designed to scale and accommodate all relevant data for a trial. Be a part of this innovative advancement for speeding up the process of getting new treatments to market.
The role is remote, based in Europe and will require travel within the region. You can also work from one of our offices if you prefer to, in Paris, Oxford, London, Berlin, Frankfurt, Budapest, Milan or Barcelona.
What You'll Do
- Develop custom listings based on customer data cleaning requirements using SQL-based language
- Configure and support data ingestions (imports) into Veeva CDB
- Collaborate with clinical data providers (Central Laboratories, ECG, eCOA, IRT, etc.) to receive data and test the transfer based on requirements.
- Provide mentoring to customer programming / configuration teams
- Discuss Veeva CDB best practices with customer teams, leveraging industry knowledge regarding Clinical Data Programming
Requirements
- 5+ years of experience in Clinical Data Programming (EDC Development, SAS, SDTM, etc.)
- Prior experience in programming languages such as (SAS, R, JSON, Python, SQL) with the ability to learn new programming languages (SQL based language)
- Working knowledge of clinical trial processes specifically as they relate to data collection and review
- Proven ability to manage diverse stakeholders, and ensure delivery to a high degree of satisfaction
- Proven ability to work independently in a dynamic, fast-moving environment, but also as part of a team where you need to “roll up your sleeves” to implement a clinical solution
- Ability to travel up to 25%
Nice to Have
- Knowledge of CDISC Standards CDASH & SDTM, ADaM knowledge
- SaaS/Cloud experience
- Life Science, computer science, change management, or related degree
- Experience with Veeva applications
- Locality to major life sciences customer hub
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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 [email protected].
