Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs)
Job title: Quality Manager MES (IFB) Job type: Permanent, Full time About the job Sanofi has decided to invest into a new large state-of-the art facility for Insulin Drug Substance in Beijing, China. For this green
Data Collections Development APAC comprises several teams who are responsible for the development of real-time systems that collect data from stock exchanges in Asia and Pacific; this data is critical to hundreds of thousands of customers
What we offer Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you
Murex is a global fintech leader in trading, risk management and processing solutions for capital markets. Operating from our 19 offices, 3 400 Murexians from over 65 different nationalities ensure the development, implementation and support of
Job Description SummaryLearn and apply practical engineering principles, build technical expertise in Electrical Engineering, and explore innovative methods while working collaboratively with a team. This role is responsible for the design and release of electrical products
Key responsibilities 重要职责 Study Start-up & Submission Execution: Lead, coordinate and manage execution of start-up activities and regulatory submissions for assigned trials Productivity Oversight: Provide local regulatory insights and support continuous improvement and innovation initiatives related
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Job Description: This position aims to serve TC revenue business activities and action plans, the intern’s contribution will bring fresh and differentiated marketing mindset and academic value of marketing tendency to Airbus training in China. ●
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
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
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
Associate Project Manager, China ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission
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 -
Pharmacovigilance Advisor Play a critical role in patient safety while ensuring compliance across one of our most important growth markets. Your new role As a Pharmacovigilance Advisor, youll be instrumental in maintaining the highest safety standards
Company: Qualcomm China Job Area:Engineering Group, Engineering Group Systems Engineering General Summary: Position Overview We are seeking an engineer specializing in the development of robotic vision perception systems. This role involves end-to-end R&D, from image processing
Company: Qualcomm China Job Area:Engineering Group, Engineering Group Systems Engineering General Summary: We are seeking an engineer with strong software development skills and a solid understanding of robotic systems, focused on designing robotic software architecture and
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
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every