Tätigkeitsbereich:Forschung & Entwicklung incl. Design Fachabteilung:Program Management AD & App Gesellschaft:Mercedes-Benz Group China Ltd. Standort:Mercedes-Benz Group China Ltd., Beijing Startdatum:01.07.2026 Veröffentlichungsdatum:23.06.2026 Stellennummer:MER00044FW Arbeitszeit:Vollzeit Bewerben Aufgaben Objective of job Lead end-to-end program management of driver assistance and automated driving
WBG Pioneer - Research & Knowledge Management InternJob #:req37536Organization:World BankGrade:T4 (No-fee)Location:Beijing,ChinaHiring Manager:Cristian Aedo Required Language(s):EnglishPreferred Language(s):Mandarin Chinese (written and spoken)Closing Date:8/12/2026 (11:59pm UTC) Description WBG Pioneers, the World Bank Group’s Internship Program, offers undergraduate and postgraduate students
Job Overview: The Senior Clinical Research Associate monitors investigational sites to ensure subject safety and provide high quality data review and reporting in compliance with the Company and/or client Standard Operating Procedures (SOPs), Good Clinical Practice
At ABB, we help industries run leaner and cleaner—and every person here makes that happen. You’ll be empowered to lead, supported to grow, and proud of the impact we create together. Join us and help run
Job Description Introduction to the job The HR People Ops(PO) team could be the best place to start your HR career journey. We are the 1st line to handle HR daily transactions and incoming employee, manager
Typical Accountabilities - Coordinate lifecycle management, enhancement, and business continuity for Study Delivery processes, systems, reporting, and technology across the clinical research portfolio. - Develop, implement, and continuously improves reporting tools, metrics, and analytical processes, identifying new opportunities
Location: Beijing-Airport, China Thales is a global technology leader trusted by governments, institutions, and enterprises to tackle their most demanding challenges. From quantum applications and artificial intelligence to cybersecurity and 6G innovation, our solutions empower critical
• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
Typical Accountabilities: - Support Global Study Leaders (GSL) and Global Study Associate Manager (GSAM) by completing delegated study work. - Initiate and lead the set-up of the electronic Trial Master File (eTMF). Maintain and close the
Job Overview: The Senior Clinical Research Associate monitors investigational sites to ensure subject safety and provide high quality data review and reporting in compliance with the Company and/or client Standard Operating Procedures (SOPs), Good Clinical Practice
Responsible for supporting the Pfizer Research & Development group Medical Information and Review, specifically: Working collaboratively with Medical and Marketing teams to review promotional, training and continuing medical education material in compliance with relevant SOPs/ regulations/
Job Summary: Provides expert technical support to the Cummins Inc. Service Channel for complex service related issues. Key Responsibilities: Leads the investigation of product or system problems, understands causal mechanisms, recommends appropriate action. Support failure analysis process
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 trials
Location:Beijing, China Job ID: R0134490 Date Posted:2026-06-29 Company Name:HITACHI ENERGY (CHINA) LTD. Profession (Job Category):Sales, Marketing & Product Management Job Schedule: Full time Remote:No Job Description: The opportunity Hitachi Energy is renowned worldwide as a specialist for
Location:Beijing, China Job ID: R0127361 Date Posted:2026-06-29 Company Name:HITACHI ENERGY (CHINA) LTD. Profession (Job Category):Legal, Compliance & Audit Job Schedule: Full time Remote:No Job Description: The opportunity Hitachi Energy is a global technology leader that is
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more
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
Company Description Sandisk understands how people and businesses consume data and we relentlessly innovate to deliver solutions that enable today’s needs and tomorrow’s next big ideas. With a rich history of groundbreaking innovations in Flash and