Beijing, Beijing, China · On-site
职位概要 作为研究中心研究者团队的成员，在研究中心遵照研究方案、商定的工作范围、GCP、申办者/公 司SOP及其他相关指南和法规的要求，来协调和执行所分配的临床试验。 职责 • 作为研究团队成员，遵照法规要求、商定的工作范围、适用的SOP、工作授权和试验方案，在 研究中心进行工作。 • 协助研究者完成可行性调查问卷和回收问卷。 • 推动研究中心启动工作：协助研究中心筛选访视，协助及时提交文件到伦理委员会进行审批 和试验用药品的发放，协助…
Skills: Clinical Research Coordination, GCP Compliance, Patient Screening, Case Report Form (CRF) Data Entry, Medical Terminology
Beijing, Beijing, China · On-site
Company Description Renesas is one of the top global semiconductor companies in the world. We strive to develop a safer, healthier, greener, and smarter world, and our goal is to make every endpoint intelligent by offeri…
Skills: Innovation Strategy, Technology Strategy, R&D Management, Market Trend Analysis, Stakeholder Management
Beijing, Beijing, China · On-site
At ABB, we help industries run leaner and cleaner—and every person here makes that happen. You’ll be empowered to lead, supported to grow, and proud of the impact we create together. Join us and help run what runs the wo…
Skills: Project Management, New Product Development, R&D Leadership, Productization, Risk Management
Beijing, Beijing, China · On-site
Job Description Summary Reporting to the Sales Manager, the Scientific Sales Representative’s primary responsibility is to manage the existing relationship of STEMCELL Technologies as well as to generate revenue in the t…
Skills: Sales Management, Business Planning, Prospecting, Cold Calling, Consultative Selling
Beijing, Beijing, China · On-site
根据试验方案、合同规定的工作范围、SOP和GCP的要求进行研究中心筛选、启动、监查和关闭访视。 可同时负责多个方案、研究中心和治疗领域内的研究中心监查工作。 对所负责的研究中心进行方案和研究相关的培训，与研究中心进行定期沟通以管理项目进行中的要求和问题。 评估研究中心工作的质量和完整性，确定研究中心是否是按照方案和适用的法规进行研究。将质量问题汇报给负责的PM和/或直线经理。 通过追踪注册申报和批复、招募和入选、病例报告表（CRF）完成…
Skills: Clinical Research Associate, Site Monitoring, GCP, SOP, Clinical Trial Management
Beijing, Beijing, China · Hybrid
China-Principal Clinical Data Standards Consultant 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-dri…
Skills: CDISC Standards, Clinical Data Management, CDASH, SDTM, ADaM
Beijing, Beijing, China · On-site
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor r…
Skills: Site Monitoring, Clinical Research, GCP, ICH Guidelines, Site Management
Beijing, Beijing, China · On-site
职衔：普药事业部-医学信息沟通代表 地点：北京 关于工作 作为我们普药事业部的医学信息沟通代表，您将加入团队，转变全球慢性病和特药疾病的医疗保健服务方式。在 General Medicines 中，您将帮助推动糖尿病、移植和免疫学领域取得有意义的成果—以患者应得的规模和紧迫性。准备好开始了吗？ 关于赛诺菲： 我们是一家以研发为驱动、以AI为动力的生物制药公司，致力于改善人们的生活并实现令人信服的增长。我们对免疫系统的深入理解以及创新的产…
Skills: Academic Promotion, Customer Management, Execution Ability, Resilience, Learning Agility
Beijing, Beijing, China · On-site
Job Description SummaryRotational Engineering Leadership program committed to growing GE's entry level, high potential talent-people with a passion for technology, a drive for technical excellence, professional skills an…
Skills: Circuit Design, Embedded Systems, FPGA, Mechanical Design, Java
Beijing, Beijing, China · Hybrid
Informed Consent Specialist II, China, office based 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-dr…
Skills: Informed Consent Development, Clinical Research, Regulatory Affairs, GCP Knowledge, Stakeholder Management
Beijing, Beijing, China · On-site
NVIDIA has been transforming computer graphics, PC gaming, and accelerated computing for more than 25 years. It’s a unique legacy of innovation that’s fueled by great technology—and amazing people. Today, we’re tapping i…
Skills: Multibody Dynamics, Robotics Simulation, GPU Accelerated Computing, Numerical Solvers, ROS 2
Beijing, Beijing, China · On-site
Key Responsibilities As an AI Scientist/Senior Scientist, you will: Design, develop, benchmark, and implement advanced AI/ML models (self-supervised and supervised) for biologics discovery and engineering, including prot…
Skills: AI/ML Modeling, Protein Language Models, Structure Prediction, Python, PyTorch
Beijing, Beijing, China · On-site
The Emerging Tech Standard Delivery Team drives the adoption of advanced technologies and develops enterprise‑ready solutions for D&A Operations. In this role, the individual partners with Operations and Technology teams…
Skills: Python, Machine Learning, Natural Language Processing, Large Language Models, RAG
Beijing, Beijing, China · On-site
Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requiremen…
Skills: Site Activation, Regulatory Document Preparation, Clinical Research, Quality Control, Project Planning
Beijing, Beijing, China · On-site
We go beyond the obvious, using intelligence, passion and creativity to inspire new thinking and shape the world we live in. To start a career that is out of the ordinary, please apply... Job Details Main Responsibilitie…
Skills: Market Research, People Management, Client Servicing, Business Development, Research Methodology
Beijing, Beijing, China · On-site
experimental execution in support of sample analysis and validation. Responsible for root cause analysis, troubleshooting, and supporting process improvements. Essential Functions • Responsible for performing and documen…
Skills: Analytical Procedures, Root Cause Analysis, Troubleshooting, Data Analysis, LIMS
Beijing, Beijing, China · Hybrid
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less in…
Skills: Audit Management, Compliance Management, Compliance Risk, Consulting, Controls Compliance
Beijing, Beijing, China · On-site
Job Overview Direct and manage the execution of the strategic, operational and financial delivery of required Site Activation activities, including but not limited to Site ID and Selection, Ethics and Regulatory processe…
Skills: Project Management, Site Activation, Regulatory Compliance, Clinical Trial Management, Contract Negotiation
Beijing, Beijing, China · On-site
职衔：普药事业部-医学信息沟通代表 地点：南阳 关于工作 作为我们普药事业部的医学信息沟通代表，您将加入团队，转变全球慢性病和特药疾病的医疗保健服务方式。在 General Medicines 中，您将帮助推动糖尿病、移植和免疫学领域取得有意义的成果—以患者应得的规模和紧迫性。准备好开始了吗？ 关于赛诺菲： 我们是一家以研发为驱动、以AI为动力的生物制药公司，致力于改善人们的生活并实现令人信服的增长。我们对免疫系统的深入理解以及创新的产…
Skills: Academic Promotion, Customer Management, Execution Ability, Resilience, Learning Agility
Beijing, Beijing, China · On-site
Job Description Location: Beijing& Shanghai Our Company seeks individuals to provide leadership and experience in conducting early clinical research in China. One of the most important missions of clinical research in Ch…
Skills: Clinical Development, Clinical Research, Clinical Trial Development, Clinical Trials Monitoring, Drug Development
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Coordinate and execute clinical trials at research centers in accordance with protocols, GCP, and SOPs. Responsibilities include subject screening, managing trial supplies, data entry into case report forms, and coordinating site initiation and closure.
Requires an associate degree or higher in clinical medicine, pharmacology, nursing, or a related healthcare field. Candidates should have less than one year of CRC experience and a basic level of English proficiency.
职位概要 作为研究中心研究者团队的成员，在研究中心遵照研究方案、商定的工作范围、GCP、申办者/公 司SOP及其他相关指南和法规的要求，来协调和执行所分配的临床试验。
职责
• 作为研究团队成员，遵照法规要求、商定的工作范围、适用的SOP、工作授权和试验方案，在 研究中心进行工作。
• 协助研究者完成可行性调查问卷和回收问卷。
• 推动研究中心启动工作：协助研究中心筛选访视，协助及时提交文件到伦理委员会进行审批 和试验用药品的发放，协助研究中心启动访视。 • 协助研究者进行受试者筛选和入组研究。
• 得到研究者授权后，根据法规和GCP的要求，协助研究者顺利完成方案要求的随访和步骤：如 制定计划、清点核对药品和其他协调工作。
• 在研究中心协助研究者管理试验用药品、研究物资和实验室样本。
• 在商定的工作范围内，参加研究者会、监查访视、稽查和其他会议。
• 协助研究者归档研究资料，并提交至伦理委员会或其他权威机构。
• 准确地将原始文件中的数据填写到病例报告表，并协助query的解答。
• 推动研究中心关闭：协助研究中心关闭访视、试验用药品和研究资料的回收，以及研究资料 的归档。
• 创建和维护日常工作报告和其他工作文件。 • 根据工作需要，可能需要不定时出差或暂时借调至其他城市。
• 完成分配的其他任务。
所需知识、技能和能力
• 了解临床研究的基本知识和适用的法规要求。
• 熟悉医学术语。
• 良好的人际沟通及组织能力。
• 熟练使用微软办公软件。
• 熟练的中文说写能力。要求基本的英语水平。
• 能独立完成任务，根据优先级选择重点，寻找资源，能解决问题，适应在团队中工作。
• 能够严格保密。
学历和经验要求
• 大专及以上学历，临床医学、药理学、护理、卫生保健或其他医学相关专业。
• 未满1年的临床研究协调员从业经验。
• 临床研究或医药行业工作/实习经验。
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
There are currently 223 open science & research positions in Beijing, China listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include IQVIA, ICON plc, Sanofi, AstraZeneca, MSD, among others. Browse the listings above to see every active employer.
Yes — 46 of the 223 open science & research positions offer remote or hybrid work (10 remote, 36 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
