Regulatory Authorities Jobs in China

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 DescriptionPrepares review and coordinates submissions (MoH EC applications if e.g. gene therapy approvals safety dossiers import license) in alignment with global submission strategy.Provides strategy advice (MoH &/or EC) t...

Job Description职务描述Brief Description of PositionThe role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations Our company policies and...

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...

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...

JOB DESCRIPTION:Major Responsibilities/Activities:Directly supporting EM MD and DVP China functionally on daily basis the Medical Affairs Director will lead the strategies and goals for medico marketing activities across China ensuring compliance with all applicable Company policies and industry s...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionPrepares review and coordinates submissions (MoH EC applications if e.g. gene therapy approvals safety dossiers import license) in alignment with global submission strategy.Provides strategy advice (MoH &/or EC) t...

Job Purpose and Impact The Food Safety Quality and Regulatory Site Senior Supervisor will ensure that all final product shipments meet or exceed the company customer and regulatory this role you will maintain and continuously improve the product safety culture at the site as well as the management...

The role We are seeking highly motivated and skilled HK IPO/ Capital Markets Associates to join our dynamic team in Beijing and Shanghai. The successful candidate will be involved in a wide range of Greater China IPO transactions. This role requires a deep understanding of financial markets as well...

- Partner with EHS Manager & regional EHS Leads to run large scale global EHS projects and future initiatives. - Lead EHS support for retail operations in Beijing ensuring compliance with national and local regulations.- Develop and implement EHS policies and programs in alignment with Chinese la...

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...

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...

Senior Finance ManagerRole summary - Payoneer is looking for a Senior Finance Manager to join our extremely fast-growing global Fintech business in China. The ideal candidate will be comfortable in a fast-paced multi-tasking and high energy environment. Location: GuangzhouOn-siteFull-timeWhat youll...

At Fortrea we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship/apprenticeship PV internits a launchpad for your future.As an Intern/ApprenticePV internyoull join a global team where curiosity motivation and fresh ideas are celebrated. Youll wo...

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...

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...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionPrepares review and coordinates submissions (MoH EC applications if e.g. gene therapy approvals safety dossiers import license) in alignment with global submission strategy.Provides strategy advice (MoH &/or EC) t...