Clinical Research Jobs in China

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...

Position SummaryThe Database Operator (DBO) is responsible for maintaining and enhancing IQVIAs healthcare reference databases including Healthcare Professionals (HCPs) Healthcare Organizations (HCOs) and related healthcare entities. The role requires conducting detailed research validating informat...

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Please provide your CV in EnglishResponsibilities:Ad...

Job DescriptionThis role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations company policies and procedures quality standards and adverse event reporting requirements internally and ext...

Job OverviewReview assess and process Safety data and information across service lines received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior oper...

Job TitleAdvisory MR Clinical ScientistJob DescriptionYour role:Collaborate with radiologists to conduct clinical application research on MR / AI participate in the design of scientific research projects follow-up on progress contribute to SCI paper writing and promote the output of academic achieve...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Operations Strategy Consultant Make an Impact at the Forefront of Innovation and Thermo Fisher China Growth strategy.At Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a...

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Please provide your CV in EnglishResponsibilities:Ad...

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) tea...

Job OverviewPerform/Assist the Data Manager in managing various data management projects as per sponsor requirements and to provide efficient quality management products. Support coordinate with other departments sites and sponsors as and when necessaryEssential Functions Perform/Assist regular Data...

作为研究团队成员遵照法规要求商定的工作范围适用的SOP工作授权和试验方案在研究中心进行工作 协助研究者完成可行性调查问卷和回收问卷 推动研究中心启动工作协助研究中心筛选访视协助及时提交文件到伦理委员会进行审批和试验用药品的发放协助研究中心启动访视 协助研究者进行受试者筛选和入组研究 得到研究者授权后根据法...

Job Overview:The Clinical Research Associate I MEA (CRA I MEA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CRA I MEA shall reflect their experience and level of contribution which they can m...

Essential FunctionsManage about 1 local Prime site6 other strategic sites which may locate in the other cities. Works under moderate supervision to develop new alliance site and maintain the cooperation.Support implementation of the IQVIA Prime Site strategy works under moderate supervision to maxim...

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...

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 OverviewDirect and manage the execution of the strategic operational and financial delivery of required Site Activation activities including but not limited to Site ID and Selection Ethics and Regulatory processes and Site Contracting for assigned studies as determined by Company scope of work a...

Responsible for FL scanner product line managementincluding portfolio management and global BU contact and overall revenue achievement for overall LBS. Conduct Scientific Insight & Solution Development Conduct in-depth analysis of target markets (e.g. drug discovery preclinical development Pharmace...

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...

根据试验方案合同规定的工作范围SOP和GCP的要求进行研究中心筛选启动监查和关闭访视 可同时负责多个方案研究中心和治疗领域内的研究中心监查工作 对所负责的研究中心进行方案和研究相关的培训与研究中心进行定期沟通以管理项目进行中的要求和问题 评估研究中心工作的质量和完整性确定研究中心是否是按照方案和适用的法规进...

JOB OVERVIEWProvide support and guidance to less experienced members of an HR team in their day-to-day operational roles. Support the continuous improvement of the HR function through development and implementation for all HR programs in an assigned geography or assigned business line. With limited...