Guidance Documents Jobs in Shanghai

Job Description SummaryJob OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Managem...

Job OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provi...

Job OverviewManage Client or Project specific 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) for specified projects. Manage and process expedita...

JOB DESCRIPTION:Primary Function职责概述To operate the registration in compliance for China and select countries in Asia Pacific regionTo ensure the registration schedule to meet the business development requirementMajor Responsibilities主要职责1. Lead and complete regulatory registrations to ensu...

Job Overview:Assist with the 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 expendable adverse...

Job Description SummaryPrimarily responsible for oversight of all activities related to the global case processing of Individual Case Safety Report (ICSR) information from all sources including post-marketing clinical trials and published literature. This role is also responsible for compliance root...

Job Description SummaryPrimarily responsible for oversight of all activities related to the global case processing of Individual Case Safety Report (ICSR) information from all sources including post-marketing clinical trials and published literature. This role is also responsible for compliance root...

Roche fosters diversity equity and inclusion representing the communities we serve. When dealing with healthcare on a global scale diversity is an essential ingredient to success. We believe that inclusion is key to understanding peoples varied healthcare needs. Together we embrace individuality and...

GALD) 901981 Job Title: Regulatory Affairs SupervisorLocation: Shanghai/ Beijing ChinaJob DescriptionManage registration dossiers. Ensure accurate and timely preparation of regulatory submissions of new products variation and maintenance of existing registration to obtain timely approval of product...

Job OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provi...