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
Veeva Systems is looking for a Project Manager to join our Randomization & Trial Supply Management (RTSM) team. As a Project Manager, you will be the primary point of contact with the client, including leading client meetings and training sessions and highlighting the RTMS modules, which will deliver an effective, user-friendly RTSM system for end-users included in the study. Exceptional writing, editing/formatting, organization, and time management skills are a must.What You'll DoReview protocols and include required modules in the User Requirements Specification (URS)Perform highly skilled duties such as creating, reviewing, coordinating, and managing a variety of deliverables (including, but not limited to, timelines, KOM, URS, Communication Manual, Requirements for Subject Randomizations, and Clinical Trial Material Lists for assigned projects, User Acceptance Testing, and system set up)Ensure established timelines are metFacilitate and troubleshoot any issues associated with managing the delivery of RTMS systemsProvide technical advice and assistance to other project managers, developers, validation, and customer support staffResponsible for Tier 3 on-call coverage (24/7/365)Acquire new knowledge and enhance your skillsRequirementsFour-year degree or equivalent experience2+ years of Project Management experience within the Clinical Trial IndustryAbility to take the initiative and work proactivelySuperior organizational and communication skillsWorking Knowledge Microsoft OfficeProven ability to work independently in a dynamic, fast-moving environment but also as part of a teamA logical approach to problem-solving and an excellent eye for detailExcellent verbal and written communication, interpersonal, and presentation skillsAbility to travel (~5-10%)Nice to HaveWorking Knowledge of RTSM/IRT/IVRS/IWRS/IXRSWorking Knowledge of FDA E6, E8, and 21 CFR Part 11Working Knowledge of Subject Randomizations and Clinical Trial Material listsAudit PreparednessGoogle Docs#RemoteCroatia
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.
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