RTSM Project Manager

Veeva is a mission-driven organization that aspires to help our customers in Life Sciences and Regulated industries bring their products to market, faster. We are shaped by our values: Do the Right Thing, Customer Success, Employee Success, and Speed. Our teams develop transformative cloud software, services, consulting, and data to make our customers more efficient and effective in everything they do. Veeva is a work anywhere company. You can work at home, at a customer site, or in an office on any given day. As a Public Benefit Corporation , you will also work for a company focused on 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 Do Review 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 met Facilitate and troubleshoot any issues associated with managing the delivery of RTMS systems Provide technical advice and assistance to other project managers, developers, validation, and customer support staff Responsible for Tier 3 on-call coverage (24/7/365) Acquire new knowledge and enhance your skills Requirements Four-year degree or equivalent experience Two+ years of Project Management experience within the Clinical Trial Industry Ability to take the initiative and work proactively Superior organizational and communication skills Working Knowledge Microsoft Office Proven ability to work independently in a dynamic, fast-moving environment but also as part of a team A logical approach to problem-solving and an excellent eye for detail Excellent verbal and written communication, interpersonal, and presentation skills Ability to travel (~5-10%) Nice to Have Working Knowledge of RTSM/IRT/IVRS/IWRS/IXRS Working Knowledge of FDA E6, E8, and 21 CFR Part 11 Working Knowledge of Subject Randomizations and Clinical Trial Material lists Audit Preparedness Google Docs #RemoteCroatia Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. 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. Apply for this job