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隐私政策
Sigma-Aldrich logo
默克生命科学
Expert
立即应聘

Expert

发布于 6 个月前

普通员工/个人贡献者

Bangalore, Karnataka, India
中级经验
全职员工
仅现场办公
硕士
研究与开发 (研发)
It解决方案验证
业务流程分析
制药行业
数据治理
数据管理
系统管理
英语
项目管理

薪资面议

暂无薪资依据说明。

职位详情

关于这个职位

这是一个专注于生命科学领域研发信息化的专家岗位

您将作为业务与技术之间的桥梁,负责分析研发部门的技术需求,设计并优化业务流程,并主导或支持Veeva Vault等关键信息系统的实施、配置与持续改进
您需要与业务专家、系统所有者和外部供应商紧密合作,确保解决方案满足业务目标并符合公司标准

最低要求

科学学科(如计算机科学、工程、自然科学、药学、和/或工商管理)高等学位或化学制药行业相关工作经验

良好的文档和/或数据管理背景
接受过技术项目管理方法和标准的培训
对医药市场有扎实的了解
至少3年在制药公司或服务提供商的职业经验,其中至少3年与所支持系统相关的职能业务流程经验
在管理(优选CoE Veeva系统)系统管理支持方面有经验
在数据管理(包括数据治理,优选CoE Veeva相关)方面有经验
在管理研发业务和/或技术项目(包括方法、标准和文档)方面有经验
在IT解决方案的资质确认和验证活动方面有经验
流利的英语口语和书面表达能力
具备项目管理的思维方式
具备强大的流程管理思维
具备强大的数据管理思维
对数据隐私有强烈的意识
强大的组织能力和独立工作能力
强大的利益相关者管理技能

工作职责

分析研发部门当前和未来的技术需求,推荐合适的信息学解决方案

分析并支持研发职能流程的设计和优化,在系统中实施流程改进
从主题专家处收集信息,记录业务需求,并将其转化为技术要求
实施流程/工作流设计(包括必要的业务流程分析和来自外部方的数据集成)
支持业务合作伙伴进行商业案例准备
支持系统所有者在解决方案设计、创建功能规范方面的工作
准备系统用户培训指南
为我们的Veeva Vault系统设计和实施EVA页面,作为团队成员和利益相关者信息战略的关键要素
持续向系统用户通报我们Veeva Vault系统的最新更新、相应的培训材料、联系人、新闻通讯和相关页面链接
确保所创建内容的吸引力设计以及它们对公司品牌指南的遵守

优先资格

有管理软件供应商和外部服务提供商的初步经验

AI 洞察

优缺点分析

优点

  • You gain deep, specialized expertise in Veeva Vault, a leading platform in the life sciences industry, making your skills highly valuable. Working at Merck, a global science and technology leader, provides exposure to cutting-edge R&D projects and a strong brand name for your career. The role offers a unique mix of business analysis, technical implementation, and project management, allowing for well-rounded professional development.
  • The role requires navigating complex stakeholder landscapes across R&D functions and IT, which can involve managing conflicting priorities. You must stay current with frequent updates to the Veeva Vault platform and ensure all implementations comply with strict pharmaceutical industry regulations (e.g., validation). The specificity of the role (pharma R&D + Veeva) might be perceived as niche, potentially limiting immediate opportunities outside this domain.
  • This role is ideal for a detail-oriented professional with a blend of technical and business acumen, who enjoys optimizing processes and systems within the highly regulated and impactful pharmaceutical R&D environment.

缺点 / 挑战

暂无明显挑战项

角色解读

  • Within the company, you could grow into a senior expert or lead roles within the IT/Informatics function supporting R&D, or transition into a dedicated Business Partner role. The deep domain knowledge in pharmaceutical R&D processes and systems like Veeva Vault is highly transferable, opening doors to senior consultant, solution architect, or product management roles within the life sciences software and services industry.
  • You will act as a bridge between R&D functions and IT, analyzing their technology needs and translating them into informatics solutions. A key part of your role involves designing, implementing, and optimizing processes within systems like Veeva Vault, including creating user interfaces (EVA pages) and managing system updates and communications. You will also support project phases from business case preparation and solution design to user training and system validation.
  • You need a strong foundation in data and document management principles, coupled with hands-on experience in administering and configuring enterprise systems, specifically Veeva platforms. Project management skills are essential for handling R&D technology projects from initiation to validation. Excellent stakeholder management and communication skills in English are required to gather requirements and liaise between technical teams and business users.

申请策略

  • Research Merck's specific business units in Life Science and their pipeline to understand the context of the R&D functions you'll support. In your cover letter, emphasize your passion for science and technology's role in healthcare, aligning with the company's 'Work Your Magic' ethos mentioned in the description.
  • Quantify your experience with Veeva Vault or similar systems (e.g., 'Administered Veeva Vault for 2 years, supporting 50+ users'). Highlight specific R&D processes you have analyzed or improved, and any projects where you translated business needs into technical solutions. Clearly list your experience with data governance, project management methodologies, and IT system validation in a regulated context.
  • If not already proficient, familiarize yourself with Veeva Vault's core modules and capabilities through official documentation or online resources. Brush up on business analysis techniques for process mapping and requirement gathering. Review fundamentals of IT validation in GxP (Good Practice) environments common in pharma.

面试指南

  • Use the STAR (Situation, Task, Action, Result) method to structure your answers, focusing on your specific actions and the measurable outcomes. For technical questions, be precise about the systems, tools, and methodologies you used. For behavioral questions, demonstrate your communication, problem-solving, and project management mindset.
  • 'Walk us through a time you analyzed a business process and recommended a system-based improvement.' 2. 'Describe your experience with managing the administration and configuration of Veeva Vault or a similar enterprise system.' 3. 'How do you approach gathering requirements from non-technical stakeholders and ensuring they are accurately translated for technical teams?' 4. 'Can you explain your involvement in the qualification or validation process of an IT system?' 5. 'Tell us about a challenging stakeholder situation you managed during a project.'
  • Prepare 2-3 detailed project case studies that showcase your skills in system implementation, process optimization, and project management within pharma/life sciences. Be ready to discuss the pharmaceutical R&D landscape and common challenges. Review key Veeva Vault functionalities and think about how they solve business problems in document and data management.

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