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Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

At Cadence, we hire and develop leaders and innovators who want to make an impact on the world of technology.Position Description:Plan and develop strategy to test/qualify SPICE simulatorsWork closely with team to enhance product quality and customer support.Build tools and setup test method to improve test process/coverage.Position Requirements:MS in...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

该职位来源于猎聘 Project Manager – Market Access Main responsibilities: Project management:  Support global or local MA projects or RWE studies under multi-cultural environment  Manager projects from start to finish including creating or supporting on preparation of protocols, project materials and associated documents  Track and report on...

ABOUT YOUWe’re seeking an ambitious Team Lead with strong communication skills, strong work ethic, and the ability and desire to work in an exciting and demanding environment. You will help us to adopt our products to the China market. ABOUT USXsolla is a global commerce company with robust tools and services to help developers solve the inherent...

该职位来源于猎聘 • Perform medical monitoring work as per project scope and Medical Monitoring Plan with a larger portion as a global/program level medical monitor. • Keep up to date with current and scientific knowledge in the medical field. • Work closely with business development and other internal stakeholders in critical appraisal of...

Key points and objectives of the positionQM China Hub takes the responsibility for consolidating and enhancing various central quality functions in China. Quality EE Satellite acts as one of the most important part of QM China Hub ensures both PbP and CBU carlines quality in terms of E/E MBOS Quality validation and release Management, OTA management, COP...

【注】此岗位为2027校园招聘岗位。如您是在非校招官网看到的招聘信息，为保证申请的完整性和反馈的及时性，请您前往校招官网(https://careersite.tupu360.com/iqvia)进行申请投递。You will experience:Develop and implement research related to Real-World Evidence (RWE) business areas (observational studies,...

Position: Learning Support Teacher Section: Middle School/High School Reports to: Director of Center for Student Development Qualifications: Bachelor’s degree or above Hours of Work: 08:00 – 17:00 on normal days Period of Appointment: Full-time Role Description / Working Relationships The Learning Support Teacher reports directly to Director of Center...

Role: Product Manager, China Reports into: VP Operations, Emerging Markets Location: Beijing, Shanghai, Guangzhou, or Shenzhen Department: Product   THE OPPORTUNITY MiQ is looking for a Product Manager to focus on localising and developing products & solutions for China. The Product Manager will support in scaling MiQ’s product offering by researching,...

Wood Mackenzie is the global leader in analytics, insights and proprietary data across the entire energy and natural resources landscape.For over 50 years our work has guided the decisions of the world’s most influential energy producers, utilities companies, financial institutions and governments.Now, with the world’s energy system more complex and...

Overview About the Role & Team This position is under the China AI Domain. Specifically focus on China Developer Ecosystem, Development tools, PaaS, Agent Infra and Opensource technologies. Creating robust and marketing leading research content, delivering consulting projects. What You’ll DoIndependent Research: Collect first hand data and...

When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer needs.  With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our...

The OVD (Overall Vehicle Design) is defining the vehicle architecture and response the geometrical integration of all related systems, modules, and components to a consistent overall vehicle (packaging).Target is to reach the overall optimum regarding function, design, ergonomics, weight, and costs plus the fulfilment of assembly, crash and service...

Objective of job：·        Developing China specific parts and manage part localization projects from styling feasibility to part release with handover to series production·        Evaluate and verify localized parts maturity as qualified components responsible person in China and serve as a contact person for both RD Germany and Joint Venture...

Typical Accountabilities- Manage the triage, evaluation, and follow-up of safety documents and clinical or post marketed adverse event information, ensuring accuracy, validity, and compliance with regulations.- Apply scientific and technical expertise in patient safety, supporting assessments, research, and regulatory reporting, while serving as a knowledge...

Job DescriptionClinical and Regulatory Strategy Developmento Drive the clinical development, expand portfolio, and speed up registrationo Get alignments with Global PDT and obtain CDRC/LDRC endorsement.o Execution clinical & registration strategyRegulatory related interaction and clinical document preparation.Accountable for protocol development, approval...