Consultant - RIM Implementation

The Role

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.

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

Requirements

• 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

Nice to Have

• Consulting experience, working with a major system integrator or software vendor
• Experience in life sciences compliance and computer systems validation requirements