Senior Project Manager – Evinova China
職位描述
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.As Senior Project Manager, you will lead a team of consultants to manage and complete configuration of Evinova’s digital health platform for our customer’s clinical trials, with a particular focus on eCOA, home supply, eConsent, remote patient monitoring, and connected devices/sensors. Your focus will be delivering high quality configured solutions on time, within budget and with the highest quality standards. You will collaborate across teams to develop and implement digital solutions that support clinical trials and enhance the efficacy of pharmaceutical products. Your role is pivotal in shaping processes and ways of working for current and future projects.Key Responsibilities: ● Develop comprehensive project plans with clear timelines, landmarks, resource allocations, and risk management strategies. ● Lead the end-to-end implementation of digital clinical research solutions, integrating our SaaS platform with wearables and mobile devices. ● Provide regular project overviews to senior management, ensuring transparency and alignment with strategic objectives. ● Collaborate with internal teams (product, IT, and quality assurance) and external partners (vendors, customers) in a matrix environment. Ensure that local requirements are incorporated into operational plans. ● Act as the point of contact for project updates, issue resolution, and escalations. ● Ensure smooth communication and coordination across all parties to drive successful project outcomes. ● Lead a portfolio of implementation projects, ensuring adherence to established project management processes and standard methodologies. ● Track project progress, monitor important metrics, and report on status, risks, and budget adherence. ● Coordinate with the global delivery team to integrate lessons learned and continuous improvements into future projects. ● Monitor and ensure quality standards are met throughout the project lifecycle. ● Identify and minimize risks proactively, implementing corrective actions as needed. ● Handle project budgets and track expenses to ensure optimal resource utilization. ● Contribute to the ongoing refinement of project management methodologies and processes. ● Leverage industry trends and project feedback to drive innovation in our project delivery approach.Essential Requirements: ● Education: Bachelor’s degree in Life Sciences, Engineering, Computer Science, Business Administration, or a related field. ● Industry Experience: ● Tech pathway: Minimum of 3-6 years of experience in SaaS delivery for data capture in clinical trials, ideally with eCOA, EDC, or RTSM systems used in Phase I-IV clinical trials.or ● Pharma/CRO pathway: 3-6 years of experience project management, including managing vendors, tasks, budgets, timelines, and risks focused on R&D and drug development processes. ● Project Management Expertise: ● Demonstrated success in implementing and managing project management methodologies and best practices in a clinical trial environment. ● Extensive experience in stakeholder management and coordinating within a matrix organization. ● Proficiency in project management methodologies and tools. ● Technical Skills: ● Extensive experience using, or deep understanding of, e-Clinical software systems. ● Proficiency in project management tools and software (e.g., MS Project, SmartSheet, Jira, Certinia, etc.). ● Familiarity with regulatory requirements and compliance standards in clinical research (e.g., 21 CFR Part 11). Understanding of Ethics Committees (EC) submission needs. ● Certifications: Project Management Professional (PMP) or equivalent certification is highly desirable. ● Communication: ● Excellent communication and organizational skills. ● Fluent English and Mandarin, both can be used as working language.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
企業簡介
阿斯利康是全球領先制藥公司,由前瑞典阿斯特拉公司和前英國捷利康公司于1999年合并而成。阿斯利康在6大治療領域為患者提供富于創新,卓有成效的醫藥產品,包括消化、心血管、腫瘤、中樞神經、麻醉和呼吸等,其中許多產品居于世界領先地位。
阿斯利康總部位于英國倫敦,研發總部位于瑞典。產品銷售覆蓋全球100多個國家和地區。2005年公司銷售收入為240億美元。
阿斯利康擁有強大的研發能力,平均每個工作日的研發投入達到1400萬美元 (2005年研發總投入為34億美元)。我們在7個國家設有11個研發機構,共有11,900名員工從事與新藥研發相關的工作。
阿斯利康擁有極具希望的早期開發產品組合,共有45個項目處于臨床前研究階段、17個項目處于一期臨床研究階段、13個項目處于二期臨床研究階段、6個項目處于三期臨床研究階段。
阿斯利康在全球19個國家有27個生產基地,共有14,000名員工致力于為客戶提供安全、有效、高質量的產品。
阿斯利康在全球共有65,000名員工,從事醫藥產品和醫療服務的研發、生產和銷售業務。
阿斯利康被列入道瓊斯可持續發展指數(全球)以及顯示企業良好社會責任度的富時社會責任指數(FTSE4Good Index)。
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職位發布日期: 2025-03-31