The Clinical Operations Program Lead plays a pivotal role to provide input to optimize trial execution, coordinate governance interactions and product strategy. This role maintains accountable to the Global & China Project Team (GPT/CNPT) for oversight
Job Title: Clinical Research Associate Job Location: China Job Overview: The CRA monitors investigational sites to ensure subject safety and provide quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures
Job Title: Senior Clinical Research Physician (SCRP) Job Location: China, homebased Job Overview: The SCRP is a Medically Qualified person without or with limited experience in a drug development/drug safety environment or medical data review. SCRP
Tätigkeitsbereich:Forschung & Entwicklung incl. Design Fachabteilung:RD China Gesellschaft:Mercedes-Benz Group China Ltd. Standort:Mercedes-Benz Group China Ltd., Beijing Startdatum:sofort Veröffentlichungsdatum:08.06.2026 Stellennummer:MER00043DM Arbeitszeit:Vollzeit Bewerben Aufgaben Objective of Job Design mule car of electrical and electronic architecture (ADAS + Infotainment)
Job Description Summary: Manager: Senior Director, Franchise Business Development, CBL Role Type: Individual Contributor Language: Fluent English & Mandarin Relocation Provided: Limited relocation available (domestic location). Please note: This role is not a fully remote position.
JLL empowers you to shape a brighter way. Our people at JLL and are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We
Work ScheduleStandard Office Hours (40/wk) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life -
About Kuoni Tumlare: At Kuoni Tumlare, we deliver truly inspiring and innovative solutions and experiences that create value both for our Partners and Society at large. Our wide portfolio of products and solutions is built on
Drug Safety Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Location:Beijing, China Job ID: R0133962 Date Posted:2026-06-11 Company Name:HITACHI ENERGY (CHINA) LTD. Profession (Job Category):Project/Program Management Job Schedule: Full time Remote:No Job Description: The opportunity Hitachi Energy Service is a trusted lifecycle partner, providing customers with
About the job Sanofi has decided to invest into a new large state-of-the art facility for Insulin Drug Substance in Beijing, China (IFB). For this green field operation, we’re enhancing our legacy of excellence and build
Company Description Do you want to develop your career and make an impact in the fast-growth, fast-moving B2B technology space? At Informa TechTarget, you’ll collaborate and grow alongside some of the industry’s most respected experts. You’ll
Company Description Do you want to develop your career and make an impact in the fast-growth, fast-moving B2B technology space? At Informa TechTarget, you’ll collaborate and grow alongside some of the industry’s most respected experts. You’ll
Job Information职位信息 Job title职位名称: Assembling & Packaging PCU Technician 组包装PCU技术员 • Location工作地点： Beijing 北京 • % Remote working and % of travel expected 远程办公和出差的概率：N/A • Job type工作类型: Full time全职 • Site/Unit 区域/事业部：Manufacturing & Supply制造与供应事业部 About the
Tätigkeitsbereich:Forschung & Entwicklung incl. Design Fachabteilung:Powertrain Design Gesellschaft:Mercedes-Benz Group China Ltd. Standort:Mercedes-Benz Group China Ltd., Beijing Startdatum:sofort Veröffentlichungsdatum:12.06.2026 Stellennummer:MER000443O Arbeitszeit:Vollzeit Bewerben Aufgaben Objective of Job: Development of battery pack mechanical system and/or component by MB inhouse
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring
Serve as SDTL Responsible for planning and leading the delivery of all components of a clinical study to time, cost, and quality from Study Specifications (SS) through study closeout activities and Clinical Study Report (CSR). Form
Serve as SDTL Responsible for planning and leading the delivery of all components of a clinical study to time, cost, and quality from Study Specifications (SS) through study closeout activities and Clinical Study Report (CSR). Form
Responsibilities: 1、Regulatory Submission Preparation & Execution Lead the preparation, review, and compilation of high-quality regulatory dossiers (e.g., CTD/eCTD format) for product registrations, variations, renewals, and other regulatory filings to NMPA and other global health authorities. Ensure accuracy, consistency, and
Work ScheduleStandard Office Hours (40/wk) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life -