Regulatory Authorities Jobs in Shanghai

In cooperation with affiliate / Area Medical teams Marketing RA Clinical and other functional areas provides leadership oversight and support for assigned products/projects. Establishes and approves scientific methods for hypotheses rational design of affiliate/Area/Global protocols and their report...

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 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...

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...

RESPONSIBILITIES: 1. Ensure a strong medical and scientific presence for AbbVie in investigational sites and key scientific centers by facilitation of clinical research and of interventional phase 1-3 trials with AbbVie drugs while supporting requests for medical and scientific information on produc...

Position Title: Sr Scientist RegulatoryPosition Type: Regular - Full-TimeGrade:Grade 05Requisition ID:39820About the role.The Senior Compliance Expert is responsible for ensuring that finished products manufactured or marketed in China comply with relevant regulations regarding product ingredients a...

Be an essential element to a brighter future.We work together to transform essential resources into critical ingredients for mobility energy connectivity and health. Join our values-led organization committed to building a more resilient world with people and planet in mind. Our core values are the...

Medical Director Clinical Pathologist - LabCorp Biopharma Laboratory ServicesFor this Shanghai-based leadership position the Medical Director/Clinical Pathologist is required to drive quality and delivery of Medical Affairs services to both internal and external customers in the APAC region and glob...

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: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...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionKey responsibilities:Prepares 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 a...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionKey responsibilities:Prepares 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 a...

Job Description SummaryAs this role you will take part in Pharmacovigilance (PV) activities.GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition turn ideas into world changing realities...

Job Description SummaryPrimarily responsible for all activities related to the Global Pharmacovigilance (GPV) Central Safety Unit (CSU) processing of Individual Case Safety Report (ICSR) information from all sources including post-marketing clinical trials and published literature. Additionally as a...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionDiscover Impactful Work:Manages the preparation review and coordination of Country Submissions in line with global submission strategy.A day in the Life:Prepares reviews and coordinates local regulatory submissions (MoH EC a...

1. Position SummaryWe are seeking a highly motivated and technically strong statistician to join our Data & Statistical Sciences (DSS) team in China as Senior this role you will provide strategic statistical leadership and support for clinical trials conducted both in China and globally including p...

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 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...