Regulatory Authorities Jobs in Beijing

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 Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

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 Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

Job Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this role ensures smo...

Job Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this role ensures smo...

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

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

Responsibilities:1Regulatory Submission Preparation & ExecutionLeadthe 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...

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 Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

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...

Some careers open more doors than others.If youre looking for a career that will unlock new opportunities join HSBC and experience the possibilities. Whether you want a career that could take you to the top or simply take you in an exciting new direction HSBC offers opportunities support and rewards...

Medical ScientistLead clinical development strategies that bring life-changing treatments to patients across Chinawhere your medical expertise directly shapes drug registration and market access.Your new roleAs a Medical Scientist youll be instrumental in driving clinical development strategy for n...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier c...

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 clinical development solution we provide is underpinned by something special - a deep conviction in...

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 DescriptionHead of Nonclinical Associate Director or DirectorLocation: Beijing/ShanghaiWe are seeking an experienced and highly motivated Head of Nonclinical to lead our nonclinical sciences team. This role provides strategic leadership and scientific oversight across toxicology pharmacology and...

Job DescriptionHead of Nonclinical Associate Director or DirectorLocation: Beijing/ShanghaiWe are seeking an experienced and highly motivated Head of Nonclinical to lead our nonclinical sciences team. This role provides strategic leadership and scientific oversight across toxicology pharmacology and...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier c...

JLL empowers you to shape a brighter way.Our people at JLL are shaping the future of real estate for a better world by combining world class services advisory and technology for our clients. We are committed to hiring the best most talented peopleand empowering them tothrive grow meaningful careers...

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 Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

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...