Project Meetings Jobs in China
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70 Jobs Found | Sort By : Relevance | Posted Date
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Senior Display Program Manager
Amazon
About the RoleWere seeking an experienced Senior Display Technical Program Manager to lead the development and delivery of cutting-edge display and touch technologies for our consumer this role youll lead cross-functional teams through complex product development cycles from concept to mass product...
Associate Director, Clinical Data Management
Iqvia
Essential Functions Define and prioritize resource requirements and manage resource assignments across projects. Monitor and manage utilization and productivity of Functional Department. Assess and document competency of staff to satisfy position responsibilities. Regularly set goals and evaluates a...
Project Manager
Vitality
Team Vitality Asia Working Pattern Full time in Hong Kong OfficeExpected start date ASAPTop 3 skills needed for this role:Project managementReporting and documentationStakeholder relationship managementWhat this role is all about: We are looking for a Project Manager to be responsible for the day-...
Fsp Vaccine Cra Ii (beijing
Fortrea
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...
Clinical Research Associate Ii
Fortrea
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...
Fsp Cra(tianjin)
Fortrea
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...
Head Of Commercial Excellence
Roche
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...
Acp Project Coordinatorglobal- Shenzhen
Vertiv Group
DescriptionPosition Title: R&D Project CoordinatorEmployment Type: Full-timeLocation: ShenzhenJob Responsibilities:Assist the R&D Project Manager with project planning schedule development and task breakdown.Track project execution coordinate resources and drive on-time project delivery.Organize reg...
Senior Ra Specialist
Thermo Fisher Scientific
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...
Manager, Project Management
Stryker
Work Flexibility: OnsiteKey Responsibilities1. Team Leadership & DevelopmentLead the day-to-day management of the technical project management team including goal setting performance evaluation talent development and succession planning.Coach and support team members to strengthen their professional...
Formulation Coordinator I
Labcorp
Position Overview:Analyzes samples and/or develops/validates methodologies for various compounds and components in compliance with SOPs and regulatory agency guidelines.Duties and Responsibilities:Organizes and conducts routine analyses in compliance with applicable methods protocols SOPs and regula...
Ci Project Engineer
Arxada
Arxada is a global leader in innovative solutions that protect our world. Our groundbreaking technologies in-depth regulatory know-how manufacturing and process development help our customers to safeguard nutrition health and infrastructure efficiently through chemistry and biotechnology that enhanc...
Sr Medical Writer
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Medical Writer - Make an Impact at the Forefront of InnovationThe Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts...
Sr Manager Medical Writing
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as an Sr Manager Medical Writing - Make an Impact at the Forefront of InnovationThe Associate Director Medical Writing oversees the regional Medical Writing staff and projects ensuring the delivery of quality product...
Principal Program Manager
Cadence Systems
At Cadence we hire and develop leaders and innovators who want to make an impact on the world of technology.We are looking for a Program Manager who will be one of our important contributors of R&D Development Projects and Customer Engagements for SSG Nanjing site.As the Program Manager for the Adva...
Fsp Cra Iishanghai
Fortrea
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...
Fso Cra Ii (shenyangchangchunzhengzhou)
Fortrea
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...
Fso Cra Ii (wuhan)
Fortrea
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...
Cra Ii
Fortrea
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...
Core Cra Ii (chengdu)
Fortrea
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...