Regulatory Submissions Jobs in China

Job Overview:Responsible for assisting with overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process exp...

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...

Job TitleSr. Clinical Development Scientist IGTJob DescriptionJob Responsibilities: Analyzes clinical trial protocols and studies ensuring adherence to regulatory requirements and alignment with strategic objectives providing recommendations for protocol optimization and enhancement. Crafts comprehe...

Job Overview:Site Navigators II plays 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...

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 II plays 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...

Job Overview:Site Navigators II plays 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...

Job Overview:Site Navigators II plays 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...

Position Summary:The manager of Regulatory Affairs & Quality Assurance is responsible for ensuring that all feed ingredients and nutrition solutions are fully compliant with both global and local feed regulations. Main accountabilities: Regulatory Affairs (RA)Lead the regulatory strategy for feed in...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

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...

Job TitleSenior Clinical Development ScientistJob DescriptionJob Responsibilities: Create or analyzes clinical trial protocols and studies ensuring adherence to regulatory requirements and alignment with strategic objectives providing recommendations for protocol optimization and enhancement. Colla...

Work ScheduleStandard Office Hours (40/wk)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 ac...

Responsibility:- Leads China clinical development strategy and delivery as part of global early development. Ensures that early oncol clinical trials for their program are designed and executed to the highest scientific and quality standards and are focused on addressing the relevant technical and/o...

Job Description SummaryAs a program manager you will lead complex hardware and system level programs end to end including new product introductions platform refreshes regulatory submissions and manufacturing transfers. The role drives cross functional execution to meet quality scope schedule and cos...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

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...