Regulatory Guidelines Jobs in Beijing

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...

Regulatory Reporting FRA Analyst Own and execute daily / monthly production of FR 2052a FRY14 FRY15 liquidity reports ensuring completeness accuracy and timeliness. Prepare and validate FDIC regulatory reports in compliance with 12 CFR 369 (FDIC reporting requirements) and 12 CFR 370 (recordkeeping...

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...

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...

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...

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...

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 trialsProductivity Oversight: Provide local regulatory insights and support continuous improvement and innovation initiatives relat...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of PPD clinical research business of Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day t...

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...

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...

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 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...

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...