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
Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The
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
What You’ll Do Account Management (DTP): Manage DTP requirements for our largest enterprise customers with highly bespoke requirements, requiring in-depth knowledge of the customer and their needs. Quality Management: Oversee account level DTP quality, ensure instructions
Tätigkeitsbereich:Forschung & Entwicklung incl. Design Fachabteilung:Body Electrical Integration, Sound, NVH & Aero Gesellschaft:Mercedes-Benz Group China Ltd. Standort:Mercedes-Benz Group China Ltd., Beijing Startdatum:01.10.2026 Veröffentlichungsdatum:17.08.2026 Stellennummer:MER00047HE Arbeitszeit:Vollzeit Bewerben Aufgaben Objective 1. Leading the sound component development in China
Job TitleSenior AI Application Architect Job Description Job title: As an important member of the R&D team, the Senior AI Application Architect will lead the architecture, governance, and technical strategy of a controlled AI Harness platform
Job ID 518811 Posted since 19-Aug-2026 Organization Global Business Services Field of work Finance Company Siemens Ltd., China Experience level Mid-level Professional Job type Full-time Work mode Office/Site only Employment type Fixed Term Location(s) Beijing -
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
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
Overview This position is located at AGs Beijing office. Please apply to another open job posting if you would like to be considered for a position outside of Beijing. About Analysis Group’s HEOR, Epidemiology, & Market Access
Company: Qualcomm China Job Area:Interns Group, Interns Group Interim Intern General Summary: General Summary This role is a 3-month internship within the Business Operations team, supporting sales, PdM and BD teams on business planning and execution
Who Are We? RZR is an AI-native advertising platform built for the next era of performance marketing. We operate at the intersection of machine learning, programmatic media, and full-funnel mobile growth, powering campaigns for some of
Job Description The Director, Safety Data Management Portfolio & Resource Operations Specialist provides leadership and governance for capacity planning, resource forecasting, and portfolio performance management across SDM (Safety Data Management). This role drives standardization of metrics,