Regulatory Documents Jobs in China
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44 Jobs Found | Sort By : Relevance | Posted Date
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Senior Manager, Regulatory Affairs
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Manager Regulatory Affairs - Make an Impact at the Forefront of InnovationThe Manager Regulatory Affairs manages a team within the department and provides innovative solutions including regulatory expertise and...
Clinical Research Assistant
Stryker
Work Flexibility: OnsitePosition summary:The Clinical Research Assistant supports the Stryker NV China Clinical Affairs team in the execution of clinical study management operational activities as well as medical writing projects.The Clinical Research Assistant executes all administrative aspects of...
Sr. Regulatory Affairs
Thermo Fisher Scientific
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...
Clinical Research Associate I Ii Fsp
Parexel
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...
Clinical Trial Coord 1
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 cou...
Clinical Trial Coord
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Clinical Trial Coordinator Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across...
Clinical Research Associate I
Parexel
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...
Medical Writer
Novo Nordisk
Department: MRQLocation: BeijingThe position Perform medical writing tasks for regulatory documents (e.g. HA consultation package bridging report clinical summaries) including Chinese version proofreading. Take overall responsibility to drive local clinical trial disclosure on specific trial/proj...
Fsp Cra(tianjin)
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Fsp Cra Ii (zhengzhou)
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Fsp Cra Ii ( Chengdu)
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Specialist, Regulatory Affairs
Abbvie
Coordinate prepare or review regulatory submissions for domestic or international projects.ResponsibilitiesList up to 10 main responsibilities for the job. Include information about the accountability and scope.Provide technical review of data or reports that will be incorporated into regulatory sub...
Fso Cra Ii (beijingtianjinjinan)
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Senior Medical Writer Early Development Services
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific you will 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 a...
Packaging & Labeling Artwork Specialist
Pfizer
JOB DESCRIPTIONPfizer ConfidentialPage 1 of 4Identifying Job InformationJOB TITLE: (Title reflected Pfizer Org Chart) Packaging & Labeling Artwork SPECIALISTREPORTS TO: (Manager Title) ALIM Global AW Strategist (or)ALIM Regional Lead (or)ALIM Market Cluster LeadDIVISION/BUSINESS LINE: Research & Dev...
Regulatory Reporting Manager
Hsbc
Some careers have more impact than others.If youre looking for a career where you can make a real impression join HSBC and discover how valued youll be.HSBC is one of the largest banking and financial services organisations in the world with operations in 64 countries and territories. We aim to be w...
Fsp Cra Iichangsha
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Fso Cra (guangzhou)
Fortrea
This role is for upcoming future opportunities that may arise at FortreaFortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when th...
Fsp Cra (xi'an)
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Senior Clinical Research Physician
Abbvie
AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across several key therapeutic areas immunology oncology neuroscience and eye c...