Clinical Research Jobs in Shanghai

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 project plans as assigned. Function as...

DescriptionTasks and Responsibilities:Function as a core team member on major projects. Develop innovative solutions for complex client needs provide regular and ad - hoc consultancy services and create client - ready presentations.Actively contribute to and at times lead new initiatives aimed at ex...

任职要求1. 设计广告等相关专业2. 具有一定的design senseprefer有相关实习经历3. 每周至少工作三天能持续实习3-6个月可以尽快入职者优先4. 熟练掌握PSAIMS office等软件工作内容1. 基于行业报告与文章美化图表与制作PPT2. 为微信推文和活动物料提供设计平面设计支持3. 市场部的其他工作IQVIA is a lea...

主要职责协助负责大中华区人力资源健康福祉项目的开展包括健康福祉活动的组织宣传与协调员工俱乐部的运营管理与供应商的沟通对接项目定期总结与宣传等 协助负责大中华区临床运营团队的学习发展项目的组织与开展 支持HRBP团队的日常工作如会议安排HR报告分析等 协助HR Leader安排的其他工作任职要求认真负责细心踏实积极主动...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when the role officially opens so we can reconfirm your interest before moving...

Summary of the Role:This role sets the strategic direction and drives the execution of organizational goals related to third-party management across the APAC region. The Sr Manager partners closely with regional supply chain operations and business leaders to deliver results aligned with broader bus...

Summary of the Role:This role sets the strategic direction and drives the execution of organizational goals related to third-party management across the APAC region. The Sr Manager partners closely with regional supply chain operations and business leaders to deliver results aligned with broader bus...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Perform site monitoring visits (selection initiatio...

Job Family DescriptionConducts statistical analyses for client reports and publications performs advanced statistical programming and biostatistical analyses and utilizes findings and insights for practical application to further business operations come across innovative findings and discoveries fo...

Essential Functions Primarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarificationsinclusion/exclusion determinations and issues o...

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

About Flexport:At Flexport we believe global trade can move the human race forward. Thats why its our mission to make global commerce so easy there will be more of it. Were shaping the future of a $10T industry with solutions powered by innovative technology and exceptional people. Today companies o...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

1. Supports the TA Head and Global TA Science Lead proposes development strategies and clinical pathways for new compound registrations in China. 2. Acts as China Local Clinical Leader to lead evidence generation working group for excellent delivery for trials in China and to assess new trial oppo...

Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations Good Clinical Practices (GCPs) ICH Guidelines AbbVie Standard Operating Pr...

1. Position SummaryWe are seeking a highly motivated and technically strong statistician to join our Data & Statistical Sciences (DSS) team in China as Senior this role you will provide strategic statistical leadership and support for clinical trials conducted both in China and globally including p...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Role Purpose: This strategic role supports Dysons high-profile government affairs agenda across Greater China with a focus on regulatory engagement policy navigation and long-term stakeholder management. The Senior Government Affairs Manager will act as a bridge between internal teams and external g...