Consultant - RIM Implementation

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 (PBC), legally bound to balancing the interests of customers, employees, society, and investors.

Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

Veeva is looking for individual leaders with consulting and system implementation experience and a passion for helping customers optimize their regulatory data and document management processes.

Veeva’s RIM suite is the industry’s only unified software solution that provides fully integrated regulatory information management (RIM) capabilities, including data and document management, submission publishing, and archival on a single cloud-based platform.

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.

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

Assist presales/sales teams in defining scope, cost and estimations.

Deep experience of Regulatory processes in Life Sciences and the relevant compliance considerations

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

Strong written and verbal communication skills in both Chinese and English

Candidate must be based in Shanghai/Suzhou and have the legal right to work

Ability to travel 10-30% within China

Consulting experience, working with a major system integrator or software vendor

Experience in life sciences compliance and computer systems validation requirements