Regulatory Submissions Jobs in Beijing

(Senior) Director ToxicologyNingbo China (Onsite Relocation Supported)Salary: $120000-$180000Pharmaron is a leading global CRO delivering integrated solutions across drug discovery preclinical development and manufacturing. With a strong international footprint and continued growth we are expandin...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Perform site monitoring visits (selection initiatio...

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...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifeResponsibilities may include the following an...

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...

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

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...

Use Your Power for PurposeOur mission is straightforward: empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Whether you are developing the framework to ensure our evidence is scientifically robust providing unbiased and medically essential expertise or ex...

Job DescriptionResponsibilitiesLead 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 regulatory requirements 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...

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...

Key responsibilitiesCMC Regulatory Strategy and Change ManagementManufacturing and Testing Practice (MTP) EstablishmentCMC Technical Assessment and Regulatory SupportSubmission and Approval of Marketed Product MaintenanceRegulatory Compliance and SystemRegulatory Policy Influence and AdvocacyCross...

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...

Accounting Manager ChinaLocation: BeijingIf youre ready to have an impact in a career that makes a difference Mölnlycke could be your next step. Youll be helping to equip medical professionals around the world with solutions to improve outcomes for patients. And youll be developing yourself in a glo...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Manager - Make an Impact at the Forefront of InnovationThe Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specifi...

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...