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  (PBC), legally bound to balancing the interests of customers, employees, society, and investors.
As a  company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.
Join us in , committed to making a positive impact on its customers, employees, and communities.
The Role
We are looking for a Computer Software Validation (CSV) professional with a specialty in clinical trial software. This role would give you the opportunity to work on a leading solution in Randomization and Trial Supply Management (RTSM) software. To excel in this role, you will require strong technical writing capabilities and the ability to simplify complex topics. 
As a member of the RTSM team, you will work closely with the Development and Project Management teams to support customer RTSM implementations in a dynamic environment. You will use your expertise to take ownership of the validation process for assigned projects and play an important role in building and maintaining product excellence for the RTSM system.What You'll DoParticipate in RTSM requirement gathering sessions with clients and RTSM team membersClosely collaborate with RTSM Development and Project Management teams to ensure requirements are defined in a clear, testable, and compliant formatEnsure requirements are adequately tested following a risk-based approachDevelop and maintain CSV deliverables, including requirements specifications, test scripts, summary reports, and trace matricesManage Validation testing cycles and resolution of issues and enhancement requestsMaintain change control documentation to ensure ongoing validation of the RTSM systemProvide technical expertise to RTSM team members in computer system validation, applicable regulations, and other quality system requirementsSupport customers as needed in RTSM validation activitiesRequirements1+ years of experience in a CSV for softwareWorking knowledge of software development cycle (SDLC)Exceptional attention to detailGood interpersonal skills and ability to communicate in English with team members and customers of varying roles and skill levelsNice to HaveWorking knowledge of GCP Guidance such as 21 CFR Part 11, EU Annex 11#LI-Remote
Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.
Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.