北京招聘

Job Summary

Tired of working with old technology? Looking for an opportunity to change how regulatory information is managed in Life Sciences? Veeva’s Vault RIM suite is the industry’s first and 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.

Veeva China is looking for Consultants who have deep regulatory expertise and a passion for helping customers optimize their regulatory data and document management process with our RIM suite of applications solutions(Vault Regulatory, Vault Submissions, Vault Submission Archive, etc.).

As a key member of our Professional Services team, the Consultant will be at the forefront of our mission and responsible for three main things:

1. Understanding our customers’ challenges and regulatory needs, translating requirements into solution design, and defining strategies for deploying our cloud-based solution for managing regulatory information and content.

2. Leading and mentoring talented project team members implementing and configuring the designed solution.

3. Becoming a customer advocate, working closely with other Veeva teams (Product, Pre-sales, Strategy) to ensure customer success today and in the future.

Opportunities are available in Shanghai, Beijing and Dalian for this role. 

Responsibilities

? Lead life sciences customers in the rapid configuration and implementation of applications to support regulatory registration, application, and content management needs in the form of the Vault RIM suite (Vault Registration, Vault Submission, Vault Submission Archive, etc)

? Define strategies and implementation programs for deploying the Vault RIM suite

? Project management including resource planning, leading and motivating a cross-functional team, and project tracking and forecasting 

? Represent R&D Professional Services across multiple engagements and workstreams (e.g., solution design and configuration, data migration, systems integration, etc.)

? Ensure customer success from beginning to end of the engagement life cycle

Requirements

? Strong desire to learn new things!

? At least Bachelor’s degree in Life Science, Computer Science, or related degree

? 4+ years of experience working with or for life sciences companies, with regulatory software solutions in regulatory operations, as a consultant, business or IT representative

? Excellent communication skills – written, verbal and formal presentation

? Abilities and willingness to “roll up your sleeves” to design and deliver a project

? Ability to work independently in a fast-moving environment

? Ability to collaborate with diverse stakeholders and ensure delivery to a high degree of satisfaction 

? Fluent English language proficiency

Nice to Have

? Direct experience with regulatory information management systems, quality information management or content management systems, such as Veeva Vault, TrackWise, OpenText, Documentum, SharePoint, Parexel, DXC, Medidata, Oracle, Bioclinica, Salesforce, Workday, SAP, etc.

? Customer service or consulting experience

? Prior experience with CTMS, eTMF and eCTD software solutions

? Prior knowledge of Clinical Trial process

? Prior knowledge in ICH guidelines, Regulatory Documentation & Regulatory Submission with experience in eCTD Submission or Publishing

? SaaS/Cloud experience

Veeva是一家总部位于美国加州，为生命科学领域客户提供系统、数据解决方案的供应商，十年前的Veeva带着对中国本土市场的憧憬来到了上海。

Veeva is one Califonia based leading IT system, data solution provider in the life science industry. With the vision and expectation of China marketing, Veeva made a big push into Shanghai in 2011.

Veeva在中国业务迅速的崛起除了Veeva产品本身的优势，也和Veeva背后每一位伙伴息息相关。在Veeva，我们坚信如果有正确的公司文化，有优秀的伙伴，那公司就会有好的产品，会健康的成长。

The booming business of China Veeva are inseparable not only from Veeva’s product success but also the employee success at Veeva.

上海办公地点：静安寺越洋广场
北京办公地点：平安国际金融中心
大连办公地点：大连软件园