罗氏促进多元化、公平性和包容性，代表我们所服务的社区。在全球范围内处理医疗保健问题时，多元化是成功的关键因素。我们认为，包容性是理解人们不同医疗保健需求的关键。我们共同拥抱个性，共同抱持对卓越护理的热情。加入罗氏，每个声音都会得到重视。 职位 Participates in study protocol development, including synopsis, consent form, CRF and amendments. With appropriate experience, the CP intern may take the lead in the above tasks under the guidance of the CPS or the CP Prepares high-quality data analyses and displays for the evaluation of clinical pharmacology data (pharmacokinetics, pharmacodynamics, safety, dose/concentration response) from clinical studies Understand the overall purpose of the designated research work within clinical pharmacology discipline. Conduct high quality data/information collection, analysis performance, outputs preparation and format polish of the research work. These statements are not intended to be an exhaustive list of all responsibilities of the individual assigned to this job, but are instead intended to describe the general nature and level of this work. All above work will be under the guidance of individual’s line manager and equivalent supervisors.