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Experience Study Jobs In Beijing (Peking) - 214 Job Positions Available

1 – 20 of 214 jobs
AstraZeneca jobs

Serve as SDTL Responsible for planning and leading the delivery of all components of a clinical study to time, cost, and quality from Study Specifications (SS) through study closeout activities and Clinical Study Report (CSR). Form a motivated and aligned

AstraZeneca  25 days ago
PAREXEL jobs

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

PAREXEL  18 days ago
Caidya jobs

1. Study management • Accountable for conducting country and study level feasibility, review Pre-Trial Assessment (PTA) output to ensure appropriate site selection in China. • Provide comprehensive operational input to the protocol design to ensure operational feasibility. •

Caidya  14 days ago
Caidya jobs

Study Manager, Oncology, Insourced to MNC 1. Study management • Accountable for conducting country and study level feasibility, review Pre-Trial Assessment (PTA) output to ensure appropriate site selection in China. • Provide comprehensive operational input to the protocol design

Caidya  14 days ago
AstraZeneca jobs

Head of RIA Clinical Development is a SET‑2 role reporting to the Head of R&D China, accountable for end‑to‑end leadership and delivery of the Respiratory, Immunology, and Infectious Disease clinical portfolios from early development through registration

AstraZeneca  27 days ago
IQVIA jobs

requests and studies, including oversight of technical processes and procedures insofar as they impact pathology interpretations. Perform microscopic analyses of laboratory assays and monitor digitization of slides. Correlate clinical information with pathology findings. Release timely reports into

IQVIA  28 days ago
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Mercedes-Benz Group AG jobs

Tätigkeitsbereich:Forschung & Entwicklung incl. Design Fachabteilung:Body Electrical Integration, Sound, NVH & Aero Gesellschaft:Mercedes-Benz Group China Ltd. Standort:Mercedes-Benz Group China Ltd., Beijing Startdatum:01.10.2026 Veröffentlichungsdatum:17.08.2026 Stellennummer:MER00047HE Arbeitszeit:Vollzeit Bewerben Aufgaben Objective 1. Leading the sound component development in China

Mercedes-Benz Group AG  27 days ago
Cider jobs

Product Manager Beijing Regular Product / Planning / Project management - Product manager Responsibilities 1、Responsible for the overall product path planning and implementation for cross-border e-commerce on PC, APP, and mobile platforms. Combine the companys core

Cider  27 days ago
ICON plc jobs

Clinical Research Associate, China ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion

ICON Plc  27 days ago
Roche jobs

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,

Roche  26 days ago
RELX jobs

Are you interested in a career as a Sales Lead? Would you like to leading a team that delivers high profile services? About our Team As the world’s leading provider of science and health information, Elsevier

RELX  26 days ago
Johnson & Johnson jobs

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our

Johnson & Johnson  26 days ago
IQVIA jobs

Job Overview Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice. Essential Functions • Collect all deliveries from loading bay, log, QC, receipt in, store and distribute as required • Maintain stock

IQVIA  25 days ago
AstraZeneca jobs

The Clinical Operations Program Lead plays a pivotal role to provide input to optimize trial execution, coordinate governance interactions and product strategy. This role maintains accountable to the Global & China Project Team (GPT/CNPT) for oversight

AstraZeneca  25 days ago
ICON plc jobs

ICON-Clinical Research Associate II/ SCRA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and

ICON Plc  26 days ago
Siemens jobs

Job ID 518811 Posted since 19-Aug-2026 Organization Global Business Services Field of work Finance Company Siemens Ltd., China Experience level Mid-level Professional Job type Full-time Work mode Office/Site only Employment type Fixed Term Location(s) Beijing - Beijing

Siemens  26 days ago
BeiGene jobs

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our

BeiGene  25 days ago
Mercedes-Benz Group AG jobs

Tätigkeitsbereich:Konzernentwicklung/-strategie Fachabteilung:Corporate Office & Trade Policy GRC Gesellschaft:Mercedes-Benz Group China Ltd. Standort:Mercedes-Benz Group China Ltd., Beijing Startdatum:15.09.2026 Veröffentlichungsdatum:20.08.2026 Stellennummer:MER00047NL Arbeitszeit:Vollzeit Bewerben Aufgaben Objective of job -Support Corporate Office in safeguarding effective corporate governance, internal control and

Mercedes-Benz Group AG  24 days ago
Shell jobs

Beijing, China Worker Type:Regular Posting Start Date:August 20, 2026 Job Description: What’s the role Join us as a Graduate at Shell China where you will embark on a comprehensive 3-year programme designed to develop future leaders.

Shell  24 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 trials according

Fortrea  21 days ago

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