Regulatory Guidelines Jobs in Beijing

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...

Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation Q2 Solutions uses its global experience and scientific expertise to...

Job DescriptionThe Safety Data Lead is responsible for the analysis and interpretation ofadverse experience (AE) reports of varying complexity in compliance with regulatory requirements and internal processes. Working under the supervision of a Manager in the Global Pharmacovigilance Case Management...

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigned. Function as...

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...

Career CategoryRegulatoryJob DescriptionJob Summary: n Develop China registration strategy and implement regulatory submissions (China IND/CTN etc.) for products within Amgens portfolio in compliance with corporate standards and local regulatory requirements. n Develop HA communication strategy for...

Career CategoryRegulatoryJob DescriptionJob Summary: n Develop China registration strategy and implement regulatory submissions (e.g. China IND/ CTN etc.) for products within Amgens portfolio in compliance with corporate standards and local regulatory requirements. n Develop HA communication strateg...

Career CategoryMedical AffairsJob DescriptionMedical Director BeOne Medicines (Beigene) CollaborationWhat you will doLets do this. Lets change the this vital role you will be a Global Medical Director in the Global Oncology Medical organization and have a direct impact on oncology programs at vari...

Work ScheduleOtherEnvironmental ConditionsOfficeJob DescriptionJob 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 cleaner an...

Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation Q2 Solutions uses its global experience and scientific expertise to...

Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation Q2 Solutions uses its global experience and scientific expertise to...

University Degree in Pharmacy Biology Chemistry or related Life SciencesMinimum 3 years experience in OTC registrations (with thorough understanding of local NMPA regulations) - ability to critically analyse and apply knowledge to develop innovative regulatory strategies. Multinational company exper...

University Degree in Pharmacy Biology Chemistry or related Life SciencesMinimum 3 years experience in OTC registrations (with thorough understanding of local NMPA regulations) - ability to critically analyse and apply knowledge to develop innovative regulatory strategies. Multinational company exper...

University Degree in Pharmacy Biology Chemistry or related Life SciencesMinimum 3 years experience in OTC registrations (with thorough understanding of local NMPA regulations) - ability to critically analyse and apply knowledge to develop innovative regulatory strategies. Multinational company exper...

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...

Job DescriptionThe Safety Data Lead is responsible for the analysis and interpretation ofadverse experience (AE) reports of varying complexity in compliance with regulatory requirements and internal processes. Working under the supervision of a Manager in the Global Pharmacovigilance Case Management...

Job DescriptionThe Safety Data Lead is responsible for the analysis and interpretation ofadverse experience (AE) reports of varying complexity in compliance with regulatory requirements and internal processes. Working under the supervision of a Manager in the Global Pharmacovigilance Case Management...