Regulatory Guidelines Jobs in Beijing
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Ssu Iii
Thermo Fisher Scientific
Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionAtThermoFisher Scientificyoulldiscover 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 healthiercleane...
Associate Regulatory Affairs Manager
Abbott
JOB DESCRIPTION:Primary Function/Primary Goals/Objectives:Secure existing drug products registration submission and approval on time to protect the business continuity.Ensure drug post-market regulatory compliance including formulation label leaflet ingredient change control promotional materials...
Sr Cas
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Country Approval 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 across 100 co...
Clinical Trial Reg Affairs Specialist
Thermo Fisher Scientific
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...
Sr Scientist, Lab Operations
Iqvia
Job OverviewResponsible for serving as a technical specialist for laboratory operations identifying and driving continuous process improvement initiatives.Essential Functions Responsible for performing and documenting all analytical procedures with accuracy consistency and timeliness in accordance w...
Patient Recruitment Delivery Lead
Iqvia
Job OverviewCollaborate with pre and post award stakeholders to manage the coordination planning and implementation of Patient Recruitment and Retention support operational plans on larger multi- region studies or programs. Communicate with sponsors and project teams to implement and monitor impact...
Regulatory Analyst Iii
Cuc Corporate Brand
Regulatory Analyst IIILocation: Hybrid remote with 2-3 per week in West Palm Beach FL location What makes us greatAt the heart of our Company is a dedication to delivering energy that drives progress. We put people first work to keep them safe and build trusting relationships.What youll be working o...
Senior Manager, Regulatory Affairs
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Manager Regulatory Affairs - Make an Impact at the Forefront of InnovationThe Manager Regulatory Affairs manages a team within the department and provides innovative solutions including regulatory expertise and...
Acra
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as an Assistant Clinical Research Associate 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 ac...
Fsp Sr Cra
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionSummary of Essential Functions:Prepares reviews and coordinates local regulatory submissions (MoH EC additional special national local applications if applicable e.g. gene therapy approvals viral safety dossiers import licen...
40966-scientist, Lab Operations
Iqvia
Job OverviewResponsible 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 and documenting ana...
Medical Writer 1
Fortrea
Job Overview:Lead writer independently responsible for the preparation of clinical study protocols and clinical study reports (CSRs) and other documents as needed for lower complexity studies. Provides support to more experienced writers with the preparation of clinical study protocols and CSRs and...