Clinical Research Associate II, China ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
At Jabil (NYSE: JBL), we are proud to be a trusted partner for the worlds top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries and a vast network
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more
Focus on the development, optimization and standardization of optical surface bonding process for extended reality smart glasses assemblies. Responsible for end-to-end bonding process solutions, including but limited to adhesive material selection, process development, fixture design and
JOB DESCRIPTION: MAIN PURPOSE OF ROLE Summarize the main purpose of the role. Individual contributor that works under limited supervision. Applies subject matter knowledge. Requires capacity to understand specific needs or requirements to apply skills/knowledge. MAIN
Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials according
Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects
Responsibilities Manage staff in accordance with organizations policies and applicable regulations, including without limitation: planning, assigning, and directing work; managing performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems;
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than
The for Cytiva is responsible for technical-scientific support to the commercial team, training and trouble-shooting to the users and strategically collaborating to drive demand generation and market share growth This position is part of the located
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionAs part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life
CRA I - Guangzhou Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate
Overview Bruker Corporation businesses are leading worldwide manufacturers of analytical measurement systems for the life sciences. For more than 50 years Bruker has followed a single idea: to deliver the best technological solution for every analytical
Job Overview Provides administrative and/or technical support. Recruitment Process 第一轮：线上测评 完成指定的线上测试，用于初步筛选。 第二轮：业务面试 与业务部门进行面谈，深入了解您的专业背景与职位匹配度。 第三轮：结果通知 招聘团队将在流程结束后，正式告知最终结果。 Essential Functions • Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors’ studies, as well as
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials according
About Four Seasons: Four Seasons is powered by our people. We are a collective of individuals who crave to become better, to push ourselves to new heights and to treat each other as we wish to
我们以玩家体验为核心，致力于用创新技术为全球玩家带来卓越的游戏体验。作为 Unpublished R&D Product 团队的一员，你将与美术、叙事、动画、技术及跨职能团队紧密合作，围绕角色设计与视觉表达开展创意探索与设计实践，推动高品质角色内容在制作流程中的高质量落地。 作为一名优秀的角色设计师，你将从设计源头塑造角色的视觉语言，与美术、叙事、动画及技术团队紧密合作，定义角色风格边界，并推动设计在实际制作与最终实现中的高质量落地。 我们希望你不仅具备出色的绘画能力，更具备系统化的设计思维与风格塑造能力，能够在创意表达与制作落地之间建立桥梁。 You will report into the Creative Director of the team. Responsibilities Character Design 负责角色设计与视觉探索，从概念草图到高完成度角色设定。 探索并定义符合产品方向的角色视觉语言，包括造型、比例、剪影、材质表现等。 输出具有高度辨识度和视觉吸引力的角色设计方案。 Design Systems & Methodology 构建角色设计逻辑，包括视觉背景、功能定位、设计原则及叙事关联。 建立并持续完善角色设计规范，包括比例体系、风格边界及细节密度控制等。 在设计中兼顾整体风格统一性与设计多样性，为长期内容扩展提供支持。 Cross-functional Collaboration 与角色美术、动画、特效及技术美术团队密切合作，确保设计方案具备良好的制作可行性及稳定表现。 提供清晰、可执行的设计交付，包括结构拆解、材质指引及设计说明。 参与评审与反馈流程，持续跟进角色从概念到最终实现的整体质量。 Quality