Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
中国，上海 | 全职 | Job ID: 11620 Position Summary: Supports clinical operational effectiveness, training enablement, vendor management and serves as a key coordination point with QA for China Clinical Operations. Works closely with study teams to ensure processes
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
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
Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing
Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients’ lives. As part of our Clinical Affairs
Job Purpose The Clinical Finance Manager serves as a key finance business partner supporting R&D China clinical trial activities and clinical development operations. The role strengthens financial governance, ensures robust financial controls and compliance, supports study financial planning and
Job TitleAdvisory Clinical Scientist Job Description Job Responsibilities: Collaborate with radiation oncologists, radiologists, medical physicists, and clinical researchers to design and conduct clinical application research, follow up research progress, and contribute to publications and academic achievements. Support clinical study setup,
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
Clinical Trial Manager II - Shanghai 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
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
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
CRA II - Beijing 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
JOB PURPOSE 工 作 目 的 Summarizes the job’s purpose or role and why it exists in the organization 概 述 工 作 的 目 的 或 角 色 及 其 在 机 构 内 的
Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of
Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of
【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: 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