Regulatory Guidelines Jobs in China

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Country Approval Specialist - Make an Impact at the Forefront of InnovationThe Senior Country Approval Specialist manages the preparation review and coordination of Country Submissions in line...

Were on a mission to change the future ofclinical research. At Perceptive we help thebiopharmaceutical industry bring medicaltreatments to the market faster.Our mission is to change the worldbut to do this we need people like you.Apart from job satisfaction we can offer you:YOURSELF Starting at 14 d...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Trainee Clinical Research Associate (CRA) Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Trainee Clinical Research Associate (CRA) Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Trainee Clinical Research Associate (CRA) Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of our PPD clinical research team youll have the opportunity to support groundbreaking studies that make a real difference in patients lives. Position SummaryAs a Medical Information Specialist I you will provides te...

Make a meaningful difference to patients around the world. From design to production our Regulatory Affairs teams help guide our innovative technologies through complex international regulatory environments. Working in partnership with external government and regulatory authorities and alongside div...

Make a meaningful difference to patients around the world. From design to production our Regulatory Affairs teams help guide our innovative technologies through complex international regulatory environments. Working in partnership with external government and regulatory authorities and alongside div...

Not just a job but a careerYokogawa award winner for Best Asset Monitoring Technology and Best Digital Twin Technology at the HP Awards is a leading provider of industrial automation test and measurement information systems and industrial services in several industries.Our aim is to shape a better f...

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 of study s...

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigned. Function as...

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigned. Function as...

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigned. Function as...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Regulatory Affairs Specialist Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials acro...

Job description - Regulatory Support SpecialistJob Summary:Collection information and prepare the documentation to support the HGRAC application and submission.Provides support and assistance in terms of reviews data for accuracy and compliance to applicable SOPs and regulations. Maintains and expan...

Position Overview:Analyzes samples and/or develops/validates methodologies for various compounds and components in compliance with SOPs and regulatory agency guidelines.Duties and Responsibilities:Organizes and conducts routine analyses in compliance with applicable methods protocols SOPs and regula...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionNeed cardiologist with CV specialty and experiences in hospital settings for at least 5 years.Industry or regulatory experiences would be a plus.JD:As part of the Thermo Fisher Scientific team youll discover meaningful work...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as Associate Director Clinical Operations Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials acro...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob Descriptionrequest physician for Cell therapy. detailed JD is not availed now. pls refer to PPD MD JD:As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our...

Job Summary:To collect document and manage pertinent data including animal observations test material administration and clinical sample collection in compliance with appropriate SOPs GLPs and regulatory agency guidelines. To monitor animal health and welfare in compliance with the Animal Welfare Ac...