世界500强 外企 学习机会 留用
Job Purpose To ensure that clinical studies are conducted at investigatorsites in compliance with; 确保临床研究在调查地点的合规性; ·  the currentapproved protocol and any protocol amendment(s), ·  ICH GCP ·  GSK WrittenStandards ·  applicable locallaws and regulatory requirement(s) so that the rights, safety and well-being of humansubjects is protected and that the reported study data is accurate, complete,and verifiable from source documents.   Key Responsibilities Fully accountable for All aspects ofsite management including ensuring completion and delivery of all localactivities required to ensure high quality set up, execution and completion ofstudies to agreed timelines and budget.Communicate progress and relevantstudy information or escalate issues of the study to the local study managementteam and other key stakeholders e.g. CRA Manager/Lead as appropriate.Accountable to acquire and maintainan optimal level of knowledge in all areas to effectively perform studyactivities.Build effective long-term collaborativerelationship, and to uphold the reputation of GSK.   Knowledge/Education/Experience A. Educational Background Scientific Degree or EquivalentExperience Any general science e.g. life science,medicine, clinical research, pharmacy etc This role requires a goodunderstanding of scientific and medical information and inability to apply thisunderstanding to the conduct of clinical research activities.Masters of Science or equivalent. Advanceddegree preferred but not essential （专业、英文优秀本科生亦可）   B. Job-related experience 1~3-year experience of clinical study monitoring orequivalent experience in the clinical research field is an asset Good English language written and verbal communicationskills. Advanced/expert level of MS Office (PowerPoint, Excel,Word & Outlook) Has some level of technical expertise.