Regulatory Submissions Jobs in Shanghai

Job TitleSenior Usability DesignerJob DescriptionJob Responsibilities: Assists in creating a usability engineering plan. Compiles Human Factors Engineering (HFE) report to showcase completion of usability activities ensuring the products safety and efficacy through documented evidence of successful...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob 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 and...

Job OverviewEngage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol standard operating procedures good clinical practice and applicable regulatory requirements.Essential Functions Complete appro...

Company Overview:At Labcorp we believe in the power of science to change lives. We are nearly 70000 people across 100 countries who are harnessing science for human good. Our work combines unparalleled diagnostic laboratories drug development capabilities and commercial innovations. Together we fuel...

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) Clinical Research Physician represents frontline scientific expertisefor assigned AbbVie TA development in China. Provides clinical science insights on portfolio assessment developmental plan formation protocol discussion trial quality and safety oversight registration approval and life cyc...

As a Study Management Associate III (Clinical Trial Manager) you will be part of a dynamic centralized study management team that is responsible for the execution of our global clinical trials and a key member of the study team. The Study Management Associate III (Clinical Trial Manager) works as an...

Work Flexibility: HybridMedical WritingPerform formal literature searches and succinctly summarize scientific content for assigned projects.Participates in post-market surveillance activities by conducting routine systematic literature reviews (e.g. screens articles against inclusion/exclusion crite...

Job PurposeApply leadership experience scientific and operational expertise in a matrix organization to provide Medical Writing Strategy to complex or multiple Therapy Area assets the design and delivery of high quality fit for purpose clinical documents including those for regulatory submissions th...

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are made withi...

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within t...

Company Overview:At Labcorp we believe in the power of science to change lives. We are nearly 70000 people across 100 countries who are harnessing science for human good. Our work combines unparalleled diagnostic laboratories drug development capabilities and commercial innovations. Together we fuel...

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...

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...

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...

BandLevel 4Job Description SummaryAbout the role: The Principal Statistical Programmer is responsible for all statistical programming aspects of a large/pivotal study several studies or project-level activities (incl. submission activities). The position is a key collaborator with biostatistics in e...

We are Covestro. We are curious. We are courageous. We are colorful. We refine chemical material solutions with game-changing products. Let us empower you to push boundaries. Join us and our 18.000 colleagues now and together we will make the world a brighter place.Main ResponsibilitiesDevelop and v...

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...

SUMMARY Brii Biosciences is seeking a highly motivated and experienced Associate Director or Director of Toxicology to join our dynamic R&D team. This role serves as the toxicology subject matter expert across Briis portfolio supporting programs from early discovery through clinical development and...