【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: Participate in the design and implementation of projects related to Real-World Evidence (RWE), healthcare data analytics, and Artificial Intelligence (AI), including data management, document development, and project support activities. Support end-to-end project
【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, survey studies, systematic reviews & meta-analysis). Design and conduct observational studies: protocol development, methodology/statistical analysis plan, feasibility analysis, data
Company Description About 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
HSBC Corporate and Institutional Banking(CIB) HSBC Corporate and Institutional Banking is a markets-led, financing-focused business that provides investment and financial solutions. Through our international network, we connect emerging and mature markets, covering key growth areas. We
HSBC Corporate and Institutional Banking(CIB) HSBC Corporate and Institutional Banking is a markets-led, financing-focused business that provides investment and financial solutions. Through our international network, we connect emerging and mature markets, covering key growth areas. We
About China Automation Beijing Discovery Center – a Lab of the Future — is AstraZenecas build of a maximally automated, end-to-end wet lab in Beijing, run as one lab-in-a-loop with the Beijing AI Centers dry-lab capabilities.
Job Responsibilities: 1. Major Duties of CTA: Support the tasks below for assigned project throughout the study: Requests payments in ACM/Ariba for study related cost Updates the trial and site information as necessary in Corporate Clinical
Job Responsibilities: 1. Major Duties of CTA: Support the tasks below for assigned project throughout the study: Requests payments in ACM/Ariba for study related cost Updates the trial and site information as necessary in Corporate Clinical
About the position We are seeking one Research Associate to join our team of Target Progression at Novo Nordisk Research Centre China. This role will support hands-on work of in vivo pharmacology for target validation and early
About the position Support the “Integrated Marketing Lead” in short/long term MKT strategic planning & campaign executions thru consumer journey from building brand awareness, likeness haloing Novo Nordisk core brand essence (e.g. Semaglutide as Originator) & key
Location: Chaoyang District,Beijing,China Major Responsibilities & Duties Become oriented with the firm’s practices, policies, and culture Be familiar with the firm’s procedures, forms, audit software, and online research tool Continue to work towards advancing knowledge of
Location: Beijing/Shenzhen,Beijing/Shenzhen,China Job Title: IT Audit Associate Reports to: IT Audit Managers/ Seniors Job Summary: As an IT Audit Associate at MaloneBailey, you will be part of a dynamic team responsible for evaluating IT systems, controls, and risks
Job Description Must have Skills : Project Management methodologies (Expert) Good To Have Skills : Financial Reporting, Qualtrics, Shanghai location Job Description : Experience range = 9-11 years. Project Context and Objectives: we are looking for
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
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
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
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory
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
Senior Statistical Programmer Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity,
About the position We are seeking one Research Associate to join our team of Target Progression at Novo Nordisk Research Centre China. This role will support hands-on work of in vivo pharmacology for target validation and early