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RIM实施顾问

雇主

Veeva Systems

地点

远程 · Remote · 美国

待遇

$USD 65,000 - USD 145,000 / annual

工作模式

远程

截止日期

1月7日

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岗位摘要

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster.

岗位职责

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.As a 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, committed to making a positive impact on its customers, employees, and communities.The Role
Veeva Systems 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.Opportunities are available within the United States for this role, which is a remote position with a preference for Eastern or Central Time Zone. If a candidate is in close proximity to an airport and able to meet travel requirements, there is no work location requirement. Qualified U.S.-based candidates are encouraged to apply.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 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
Interviewing with Veeva
We value your time and believe in a transparent hiring process. Here is the process you can expect.
Follow the application process and submit your resume.
Within 3 days, you will receive a link to a personality assessment administered by a third party.
Once you complete the assessment, our team will review your full application package and follow up via email with our decision.
If moving to the interview stage, the process is as follows:
A conversation with the hiring manager
A practical case exercise
A final conversation with our group's Senior Leader.
Once all interviews are complete, the manager will be in touch with a final decision.
Perks & Benefits
Medical, dental, vision, and basic life insurance
Flexible PTO and company paid holidays
Retirement programs
1% charitable giving program
Compensation
Base pay: $65,000 - $145,000
The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus.
Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at .Originally posted on Himalayas

申请条件

- 具备咨询和系统实施经验
- 对帮助客户优化法规数据和文档管理流程有热情
- 能够理解客户的全球法规需求
- 能够将需求转化为解决方案设计
- 能够配置基于云的解决方案以管理企业范围内的法规信息
- 具备个人领导能力
- 工作地点位于美国,远程职位,优先考虑东部或中部时区
- 如果居住在机场附近并能满足出差要求,则无工作地点限制
- 美国境内合格候选人

雇主简介

Veeva Systems 为生命科学行业提供行业云解决方案,包括应用、代理、数据和咨询服务,帮助生物制药公司加速药物开发。

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数据来源:Himalayas

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