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,
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
About Human Pharmaceutical Business With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs
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,
Senior Clinical Data Science Lead At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development
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: 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
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,
Job Description Support of the company Portfolio (85%) Lead cross-functional project teams in the strategy planning, execution, and delivery of China new product development projects. Develop project milestones and deliverables; prepare reports that summarize key progress
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At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project
The Clinician is accountable for the medical and scientific integrity of one or more clinical trials and for the safety and well-being of study participants. The role applies clinical and scientific expertise to design, execute, monitor, and interpret
Beijing, China | full time | Job ID: 11588 About the role: As a Senior Manager in Global Regulatory Operations, you will play a pivotal role in driving BioNTech’s mission to revolutionize medicine by ensuring timely
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
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
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,