
Study Design Analyst – Evinova China

职位描述
At Evinova, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big, and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.Evinova is a health-tech business, separate company within the AstraZeneca Group, accelerating the delivery of better health outcomes by propelling the life sciences sector forward in digital health, from the inside. Through our application of science-based expertise, evidence-led rigor, and human experience-driven insight, our digital solutions are deliberately crafted so that everyone can reach better health outcomes together.In this role on our Solution Delivery team, you’ll lead the design and deployment of Evinova’s platform for clinical trials. You’ll translate complex clinical protocols into system configuration, manage the design process, and ensure the successful implementation of our Unified Trial Platform. Your expertise will shape the future of clinical studies, making healthcare more efficient and accessible.Key Responsibilities:Study Implementation ● Lead the design and configuration of Unified Trial Platform, ensuring clinical protocols are effectively translated into system configuration. ● Be consultative with the sponsor team, serving as a domain expert on our digital solution and providing insights into the system capabilities, configuration options and practical application of its features in a clinical trial. ● Lead the overall study configuration and design process, implementing design best practices and using reusable assets such as eCOA libraries and translations. ● Be a close partner with internal and external partners with respect to translations, assessment licensing, integration, validation and quality control.Pre- and Post-Implementation ● Support the team on assessing upcoming clinical trials, consulting on solutions and delivery methods that best meet the study’s needs. ● Conduct risk assessment and impact analysis of new software releases, upgrades and changes ● Provide ongoing support and guidance to clinical trial and implementation teams during the deployment and post-implementation phases including addressing issues and implementing improvements as needed.Essential Requirements: ● Bachelor’s degree in relevant information technology, life science or related field preferred. ● 4-7 years of experience in building and configuring digital solutions for clinical trials; 3 years of experience specifically with eCOA systems. ● Proven senior stakeholder management skills, including negotiation, collaboration, and interpersonal leadership abilities, coupled with the ability to work collaboratively in a cross-functional setting with both internal and external partners. ● Demonstrable experience of gathering and translating business requirements into technical specifications and configurations for digital solutions used in clinical trials. ● Strong understanding of clinical trial processes and regulations with respect to study design. ● Experience with connected devices (e.g. PEF, oxygen monitors) and integrating with other clinical systems, such as IVRS, EDC, data lakes, etc. ● Excellent analytical, problem-solving, and communication skills with the ability to interact effectively with team members and customers at all levels. ● Excellent discernment and insights with sensitivity to environment. ● Strong learning capability and passion to digital clinical research. ● Fluent English and Mandarin, both can be used as working language.Desirable Requirements: ● Master degree in relevant discipline. ● Experience from Healthcare and Life Sciences, preferably with clinical trials. ● Experience of working in a global organization with complex/geographical context. ● Experience of working in a regulated environment, ideally of delivering GxP and SaMD solutions.Why Evinova (AstraZeneca)?Evinova draws on AstraZeneca’s deep experience developing novel therapeutics, informed by insights from thousands of patients and clinical researchers. Together, we can accelerate the delivery of life-changing medicines, improve the design and delivery of clinical trials for better patient experiences and outcomes, and think more holistically about patient care before, during, and after treatment. We know that regulators, healthcare professionals, and care teams at clinical trial sites do not want a fragmented approach. They do not want a future where every pharmaceutical company provides its own, different digital solutions. They want solutions that work across the sector, simplify their workload, and benefit patients broadly. By bringing our solutions to the wider healthcare community, we can help build more unified approaches to how we all develop and deploy digital technologies, better serving our teams, physicians, and ultimately patients. Evinova represents a unique opportunity to deliver meaningful outcomes with digital and AI to serve the wider healthcare community and create new standards for the sector. Join us on our journey of building a new kind of health tech business to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering innovative methods, and bringing unexpected teams together.Location: Shanghai ChinaSalary: Competitive + Excellent Benefits!So, what’s next?Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you.Where can I find out more?Our Social Media, Follow Evinova on LinkedIn Learn more about Evinova
企业简介
阿斯利康是全球领先制药公司,由前瑞典阿斯特拉公司和前英国捷利康公司于1999年合并而成。阿斯利康在6大治疗领域为患者提供富于创新,卓有成效的医药产品,包括消化、心血管、肿瘤、中枢神经、麻醉和呼吸等,其中许多产品居于世界领先地位。
阿斯利康总部位于英国伦敦,研发总部位于瑞典。产品销售覆盖全球100多个国家和地区。2005年公司销售收入为240亿美元。
阿斯利康拥有强大的研发能力,平均每个工作日的研发投入达到1400万美元 (2005年研发总投入为34亿美元)。我们在7个国家设有11个研发机构,共有11,900名员工从事与新药研发相关的工作。
阿斯利康拥有极具希望的早期开发产品组合,共有45个项目处于临床前研究阶段、17个项目处于一期临床研究阶段、13个项目处于二期临床研究阶段、6个项目处于三期临床研究阶段。
阿斯利康在全球19个国家有27个生产基地,共有14,000名员工致力于为客户提供安全、有效、高质量的产品。
阿斯利康在全球共有65,000名员工,从事医药产品和医疗服务的研发、生产和销售业务。
阿斯利康被列入道琼斯可持续发展指数(全球)以及显示企业良好社会责任度的富时社会责任指数(FTSE4Good Index)。
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职位发布日期: 2025-03-31