Consultant - Veeva RIM Professional Services

Job description

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 $3B 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](https://medium.com/@peter.gassner/public-benefit-corporation-pbc-486e1e9508a6) (PBC), legally bound to balancing the interests of customers, employees, society, and investors. As a [Work Anywhere](https://careers.veeva.com/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](https://www.youtube.com/watch?v=TaPSP8cCSKY&ab_channel=Forbes), committed to making a positive impact on its customers, employees, and communities. ### The Role Veeva is looking for Consultants with deep regulatory expertise and a passion for helping customers improve their process for Regulatory Information Management (RIM), submission management, publishing, and submission archiving. We want team members ready to challenge the status quo; you’re ready to transform businesses. As a member of our Professional Services team, you will be responsible for understanding our customers’ global regulatory needs, translating requirements into solution design, and configuring our cloud-based solution for managing regulatory information across the enterprise. This is a remote, full-time permanent role with Veeva with a location preference in Hyderabad, Mumbai, Bengaluru, or Pune. ### What You'll Do - Guide life science customers in the configuration and implementation of Veeva’s Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing) to streamline global regulatory processes - Lead configuration requirements workshops, design, and document, as well as prototype and deploy solutions - Program and project management, including resource planning, leading and motivating a cross-functional team - Communicate between the project team, customer, and internal stakeholders ### Requirements - 3+ years experience working with or for organizations in life sciences or healthcare either as a consultant, business, or IT representative - Technical abilities and willingness to “roll up your sleeves” to design, configure, and implement a RIM solution - Ability to collaborate and communicate excellently with diverse stakeholders - Team player with strong organization skills and an ability to act with speed in a complex environment - Ability to travel (25% -50%) as required by the business ### Nice to Have - Consulting experience, working with a major system integrator or software vendor - Knowledge of drug development, Regulatory Affairs, or Regulatory Operations - Experience in life sciences compliance and computer systems validation requirements ### Perks & Benefits - Health and wellness programs - Life Assurance - Veeva charitable giving program - Additional annual leave over Christmas break