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 are at the
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 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
Typical Accountabilities Major Responsibilities Build up the team spirit, including develop team style and behaviour Contribute to efficient SMM organisation and its functioning at country level by working closely with responsible SMM Director Plan and organise
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
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 solution
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
ICON-Beijing- Clinical Research Associate I/II 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
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 across
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Thermo Fisher Scientific Inc. is a premier company that is dedicated to enabling our customers to make the world healthier, cleaner, and safer. We are a team of 100,000+
Clinical Research Associate II, 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 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 solution
【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
【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
【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 analysis,
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 solution
About the job As Associate Health Value Translation (HVT) Lead within our Patient Driven Medicines Development (PDMD) function, you’ll represent the department at the Global Project Team and be accountable for the Integrated Patient Disease Strategy (PDS) across
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as an Associate Manager Clinical Operations - Make an Impact at the Forefront of Innovation The Associate Manager Clinical Operations oversees the daily line management responsibilities of the assigned team. This role
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750