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All Source Analysis Jobs In Beijing (Peking) - 32 Job Positions Available

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Canva jobs

Company Description 该岗位现面向所有经验阶段的候选人开放,包括社会招聘、应届毕业生,同时开放实习生岗位。工作地点为北京。欢迎申请,期待你的加入! Notice: This position is open to candidates at all experience levels, including experienced candidates, graduates, as well as internship opportunities. The role is based in Beijing. We welcome your application and look forward to

Canva  28 days ago
Fortrea jobs

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

Fortrea  27 days ago
Fortrea jobs

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical

Fortrea  27 days ago
MSD jobs

Job Description The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Global Pharmacovigilance

MSD  26 days ago
MSD jobs

Job Description The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Global Pharmacovigilance

MSD  26 days ago
MSD jobs

Job Description The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Global Pharmacovigilance

MSD  26 days ago
MSD jobs

Job Description The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Global Pharmacovigilance

MSD  26 days ago
RWE jobs

RWE Supply & Trading (Shanghai) Co. Ltd. To start as soon as possible, full time /fixed term Functional area: Commercial / Trading About the role As a Commodity Analyst, you possess a comprehensive understanding of commodity

RWE  21 days ago
RWE jobs

RWE Supply & Trading (Shanghai) Co. Ltd. To start as soon as possible, full time /fixed term Functional area: Commercial / Trading About the role As a Data Scientist, you will apply advanced data, programming and

RWE  21 days ago
Fortrea jobs

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical

Fortrea  21 days ago
Flexport jobs

About Flexport: At Flexport, we believe global trade can move the human race forward. That’s why it’s our mission to make global commerce so easy there will be more of it. We’re shaping the future of

Flexport  18 days ago
Flexport jobs

About Flexport: At Flexport, we believe global trade can move the human race forward. That’s why it’s our mission to make global commerce so easy there will be more of it. We’re shaping the future of

Flexport  18 days ago
LILT jobs

Linguist - Traditional Chinese (Taiwan) - UI Technical/Marketing/Product Description - Remote About the Opportunity We are expanding our talent network and seeking skilled Traditional Chinese (Taiwan) professionals with expertise in user interfaces, marketing localization, and retail

LILT  18 days ago
MSD jobs

Job Description The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Global Pharmacovigilance

MSD  17 days ago
MSD jobs

Job Description The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Global Pharmacovigilance

MSD  17 days ago
Coupang jobs

Senior Staff/Staff Machine Learning Engineer-LLM Company Introduction We exist to wow our customers. We know we’re doing the right thing when we hear our customers say, “How did we ever live without Coupang?” Born out of

Coupang  14 days ago
Ericsson jobs

Join our Team What you will do: Board power solution and design for radio products, Baseband products and network router products. DCDC power solution design, including lightning protection, polarity protection, hot-swap, EMC filter, power stage and

Ericsson  13 days ago
Cummins jobs

Job Summary: Leads the Plant Product Quality Council process to improve quality, reduce warranty payments, and improve customer satisfaction across multiple plants or for a business unit. Key Responsibilities: Directs multiple teams that plan, track, and

Cummins  12 days ago
Fortrea jobs

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical

Fortrea  12 days ago
Fortrea jobs

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical

Fortrea  11 days ago

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