Project Meetings Jobs in Beijing

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...

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...

Product & Process Development: Champion the Product Development Process: Lead engineering development of powder metallurgy components and manufacturing processes: Develop and optimize powder metallurgy processes tooling concepts and manufacturing parameters: Support process validation and product la...

Product & Process Development: Champion the Product Development Process: Lead engineering development of powder metallurgy components and manufacturing processes: Develop and optimize powder metallurgy processes tooling concepts and manufacturing parameters: Support process validation and product la...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionJoin Us as a Principal Country Approval Specialist - Make an Impact at the Forefront of InnovationThe Principal Country Approval Specialist manages the preparation review and coordination of Country Submissions in...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionJoin Us as a Principal Country Approval Specialist - Make an Impact at the Forefront of InnovationThe Principal Country Approval Specialist manages the preparation review and coordination of Country Submissions in...

Job OverviewDevelop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files tables and figures. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Communicate with s...

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...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier c...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier c...

Job DescriptionGeneral/Position SummaryThe Senior Specialist will provide operational support to the Global Meetings and Events team and the broader Corporate Services function. This role ensures the seamless execution of multiple complex projects by supporting operational excellence optimizing proc...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Regulatory Affairs Specialist Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials acro...