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 Description Responsibilities Lead Regulatory CMC Policy & Intelligence efforts to effectively navigate the regulatory landscape, advocate for CMC policies, and contribute to achieving strategic policy objectives. Develop and implement CMC policy strategies that align with
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
Job title职位名称: Process, Plant and C&Q Engineer 工艺工程师 Location工作地点： 北京 About the job工作职责 Our Team我们的团队： Manufacturing & Supply consists of 3 manufacturing platforms based on global business units, as well as supporting functions of Quality, Market
Ankura is a team of excellence founded on innovation and growth. This position supports Ankura Business Services, our internal support function About Ankura Ankura is an independent global expert services and advisory firm that helps clients
Job Overview Responsible for performing a variety of technical procedures and experimental execution in support of sample analysis and validation. Responsible for root cause analysis, troubleshooting, and supporting process improvements. Essential Functions • Responsible for performing
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
Medical Writer Lead the story of life-changing treatments from research to reality—where your words bridge science and hope for millions. Your new role As a Medical Writer, youll play a critical role in bringing our innovative
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 Summary: Responsible for assessing, defining and championing the IT architecture strategies, principles, policies and standards in alignment with the companys IT strategy and governing their use; coordinates with project teams to create, document, assess and/or validate
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 Machine Learning Engineering General Summary: Job Description About us: We are Qualcomm AI Research that are advancing AI to make its core capabilities – perception, reasoning, and action