MSD R&D Innovation Centre

Job DescriptionBiomarker Operation Senior Manager/Associate DirectorLocation: Shanghai/BeijingWe are seeking a highly motivated scientist to drive clinical biomarker/diagnostic assay/lab setup to support clinical development programs across therapeutic areas in China.Key responsibilit

Job DescriptionBiomarker Operation Senior Manager/Associate DirectorLocation: Shanghai/BeijingWe are seeking a highly motivated scientist to drive clinical biomarker/diagnostic assay/lab setup to support clinical development programs across therapeutic areas in China.Key responsibilit

Job DescriptionThe CTA is an administrative support role for clinical trials. The role responsibilities include but not limited to the following activities:Basically Safety reports distribution and tracking. TMF support for country level document uploading to eTMF assist with eTMF rec

Job DescriptionThe CTA is an administrative support role for clinical trials. The role responsibilities include but not limited to the following activities:Basically Safety reports distribution and tracking. TMF support for country level document uploading to eTMF assist with eTMF rec

Job DescriptionBrief 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 polic

Job DescriptionBrief 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 polic

Job DescriptionPosition Title: Sr. Manager Operation Support GCTODepartment: Global Clinical Trial Operations (GCTO)Brief Description of PositionSERVICE PROVIDER OVERSIGHTEnd-to-End Local Service Provider Oversight:Assess GCTO China business needs and collaborate with Global Procureme

Job DescriptionPosition Title: Sr. Manager Operation Support GCTODepartment: Global Clinical Trial Operations (GCTO)Brief Description of PositionSERVICE PROVIDER OVERSIGHTEnd-to-End Local Service Provider Oversight:Assess GCTO China business needs and collaborate with Global Procureme

Job DescriptionBrief 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 polic

Job DescriptionBrief 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 polic

Job DescriptionAssociate Director Clinical Research Early PhaseLocation: Beijing& ShanghaiReport to: CR group 1 leadOur Company seeks individuals to provide leadership and experience in conducting early clinical research in China. One of the most important missions of clinical resear

Job DescriptionAssociate Director Clinical Research Early PhaseLocation: Beijing& ShanghaiReport to: CR group 1 leadOur Company seeks individuals to provide leadership and experience in conducting early clinical research in China. One of the most important missions of clinical resear

Job DescriptionJD AD Clinical Research Early PhaseLocation: ShanghaiOur Company seeks individuals to provide leadership and experience in conducting early clinical research in China. One of the most important missions of clinical research in China is to conduct innovative clinical r

Job DescriptionJD AD Clinical Research Early PhaseLocation: ShanghaiOur Company seeks individuals to provide leadership and experience in conducting early clinical research in China. One of the most important missions of clinical research in China is to conduct innovative clinical r

Job DescriptionSupport of company Portfolio (85%)Independently manage product development teams from new drug early development to the life cycle management stage and integration team with external alliance partners if need.Lead cross-functional project teams in the strategy planning

Job DescriptionSupport of company Portfolio (85%)Independently manage product development teams from new drug early development to the life cycle management stage and integration team with external alliance partners if need.Lead cross-functional project teams in the strategy planning

Job DescriptionThis role is primarily accountable for the end-to-end performance and project management forassigned protocols in a country in compliance with ICH/GCP and country regulations company policies and procedures quality standards and adverse event reporting requirements inte

Job DescriptionThis role is primarily accountable for the end-to-end performance and project management forassigned protocols in a country in compliance with ICH/GCP and country regulations company policies and procedures quality standards and adverse event reporting requirements inte

Job DescriptionRole & ResponsibilityThis position serves as the role of clinical research physician who will be in charge of the Ph1 study in Chinese participants with hematological malignancies. The responsibility of this role is to provide strong capability to lead for study determi

Job DescriptionRole & ResponsibilityThis position serves as the role of clinical research physician who will be in charge of the Ph1 study in Chinese participants with hematological malignancies. The responsibility of this role is to provide strong capability to lead for study determi

Job DescriptionBrief 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 polic

Job DescriptionBrief 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 polic

Job DescriptionRole & ResponsibilityOur Company seeks individuals to provide leadership and experience in conducting early clinical research in China. One of the most important missions of clinical research in China is to conduct innovative clinical research thus broaden the indicatio

Job DescriptionRole & ResponsibilityOur Company seeks individuals to provide leadership and experience in conducting early clinical research in China. One of the most important missions of clinical research in China is to conduct innovative clinical research thus broaden the indicatio

Job DescriptionBrief 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 polic

Job DescriptionBrief 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 polic

Job DescriptionPosition title: Manager CMC Regulatory AffairsDepartment: Regulatory AffairsReport to: Associate Director of CMCLocation: Beijing/Shanghai ChinaResponsibilitiesTake CMC lead for products under clinical development and for marketed drug products. Coordinate various aspec

Job DescriptionPosition title: Manager CMC Regulatory AffairsDepartment: Regulatory AffairsReport to: Associate Director of CMCLocation: Beijing/Shanghai ChinaResponsibilitiesTake CMC lead for products under clinical development and for marketed drug products. Coordinate various aspec

Job DescriptionRole & ResponsibilityThis position serves as the role of clinical research physician who will be in charge of the Ph1 study in Chinese participants with hematological malignancies. The responsibility of this role is to provide strong capability to lead for determination

Job DescriptionRole & ResponsibilityThis position serves as the role of clinical research physician who will be in charge of the Ph1 study in Chinese participants with hematological malignancies. The responsibility of this role is to provide strong capability to lead for determination

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

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

Job DescriptionJD Senior Manager/Associate Director Clinical Research Early PhaseLocation: Beijing& ShanghaiReport to: CR Group 1 Lead of Early Clinical Research TeamOur Company seeks individuals to provide leadership and experience in conducting early clinical research in China. On

Job DescriptionJD Senior Manager/Associate Director Clinical Research Early PhaseLocation: Beijing& ShanghaiReport to: CR Group 1 Lead of Early Clinical Research TeamOur Company seeks individuals to provide leadership and experience in conducting early clinical research in China. On

Job DescriptionPosition title: Senior Manager Regulatory Affairs CMCDepartment: Regulatory AffairsReport to: Associate Director Regulatory Affairs CMCLocation: Beijing ChinaResponsibilitiesLead Regulatory CMC Policy & Intelligence efforts to effectively navigate the regulatory landsca

Job DescriptionPosition title: Senior Manager Regulatory Affairs CMCDepartment: Regulatory AffairsReport to: Associate Director Regulatory Affairs CMCLocation: Beijing ChinaResponsibilitiesLead Regulatory CMC Policy & Intelligence efforts to effectively navigate the regulatory landsca

Job DescriptionThe Safety Data Lead I is responsible for processing adverse experience (AE) reports with high quality and compliance in the global safety system for investigational and/or marketed products under the direction and supervision of a Global Pharmacovigilance Case Manageme

Job DescriptionThe Safety Data Lead I is responsible for processing adverse experience (AE) reports with high quality and compliance in the global safety system for investigational and/or marketed products under the direction and supervision of a Global Pharmacovigilance Case Manageme

Job DescriptionDo you have a passion for driving business excellence in the pharmaceutical industry Were seeking a talented IDMP (Identification of Medicinal Products) Business Analyst to play a key role in ensuring compliance with Article 57 of EU Regulation 1235/2010 (XEVMPD/IDMP) w

Job DescriptionDo you have a passion for driving business excellence in the pharmaceutical industry Were seeking a talented IDMP (Identification of Medicinal Products) Business Analyst to play a key role in ensuring compliance with Article 57 of EU Regulation 1235/2010 (XEVMPD/IDMP) w