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
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
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
Shanghai, China | full time | Job ID: 11392 Your main responsibilities are: Lead and Drive study delivery in China Support in preparation of regular status reports to local DCO and global CTM/Platform Lead, including presentation
Responsibilities Performing site evaluation, initiation, monitoring and close-out visits, plus maintaining appropriate documentation according to a project-specific monitoring plan, ICH-GCP, and applicable regulations. Supporting the development of a subject recruitment plan. Establishing regular lines of communication plus
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 Trial Registry
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 Trial Registry
ICON-Shanghai- Senior Clinical Research Associate 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 are at
Clinical Research Associate (CRA) Job Description The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP), and applicable Project Management Plan (PMP) and local regulatory requirements. Job Responsibilities Contribute comments/input
About us BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse
Clinical Site Associate, Guangzhou, 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-driven organisation, integrity, collaboration, agility, and inclusion are
Associate Project Manager, language Services 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 are at
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 clinical development
Locations: Beijing, China Categories: Clinical Safety Req ID: 12777 Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Project Assistant to join our Clinical Safety team. This position will work on a team to
Locations: Shanghai, China Categories: Clinical Trial Management Req ID: 13020 Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience various therapeutic areas for a full-time Associate Clinical Trial
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 clinical development
Job Overview Serve in support level capacity in CDM Validation (Testing) team, to perform testing activities in CDMS environment to provide efficient, quality database as per customer requirement. Essential Functions • Conduct testing activities to validate
【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 execution and management,
【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
【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: Identify and develop Health Economics / Health Technology Assessment (HE/HTA) related methodologies and strategies. Support health economics analysis & modeling. Support product value proposition& communication, reimbursement strategies, and value-based pricing strategy. Generate