杭州招聘

• 按照验证计划、内部 SOP 和分析规程，完成生物分析/生物标志物方法学验证，并测试临床前/临床研究的生物样品。
•   按照 GLP/GCLP 规范做好实验记录和归档。及时记录偏差并报告给项目负责人。
•   与项目相关的客户沟通，审查和评估数据，参与撰写分析规程和研究报告。
•   评估项目进展情况，及时向项目负责人汇报并协助解决问题。
•   其他与公司业务相关的职责。

  

  任职要求：

•   生物学、免疫学、生物化学、药理学或相关科学领域专业的学士或以上学位。
•   愿意学习新技术，能同时执行多项任务。
•   有责任心，工作认真踏实，愿意与团队合作，遵守公司规章制度。
•   熟练使用 MS Office 和其他相关的计算机软件
  

Amador Bioscience strives to provide global-standard laboratory, clinical research, strategy consulting and regulatory filing services to biopharmaceutical companies. The laboratory services focus on PK/PD/ADA assay development and sample analysis. Amador clinical research unit specializes in innovative clinical development strategy and protocol design, and initiation and monitoring of clinical studies in China and US. In addition to R&D strategy and regulatory pathway, our consulting services perform global-standard data analysis and generate submission-ready study reports. We have successfully supported CTD filings in China and US.

With profound academic background and rich experience in R&D services in the biopharmaceutical industry, AmadorBio is a global clinical research team of pharmacologists, statisticians, bioanalytical scientists, translational & clinical scientists, medical scientists, clinical trial management experts, data management experts, quality assurance auditors, clinical trial managers and regulatory specialists. (40% of PhD, MD and PharmD, 35% of MS). AmadorBio provides professional services for more than 20 leading biopharmaceutical companies from early research and development, clinical development to regulatory submission in China and US.

AmadorBio operates in biotech hubs: San Francisco Bay Area, USA and Shanghai-Hangzhou-Suzhou region, China, providing comprehensive solutions complied with global standards and government drug inspection regulations in China and US.

The mission of Amador is to provide global-standard services facilitating the development of novel biotherapeutics.

    安渡生物致力于为生物医药公司提供全球标准的实验室、临床研究、策略咨询和监管申报服务。实验室服务专注于PK/PD/ADA方法学开发验证和样本分析。安渡生物的临床研究中心专注于为美国和中国的生物医药公司提供创新的临床研究开发策略、方案设计、启动和监查的专业服务。我们的咨询服务除研发策略和监管服务外，还可提供全球标准的数据分析并生成完备的申请报告。我们在中国和美国成功地支持了多家医药公司的CTD申请。

    安渡生物是一支具有资深学术背景、行业研发服务经验丰富的临床研究团队，拥有临床药理、数理统计、生物分析、转化科学、医学、临床运营、数据管理、质量保证审核、项目管理以及监管申报各方面专家，其中博士(PhD, MD, PharmD)占40%，硕士占35%。安渡团队致力于支持从临床前到临床各个阶段的药物开发计划。目前我们为20余家中美生物制药公司提供从早期研发，临床开发到监管申报等多个项目的专业服务。

    安渡生物在美国旧金山湾区和中国长三角地区设有办公室和实验室，提供涵盖中美及符合国际标准和政府药检规范的全方位解决方案。

    安渡生物的使命：提供全球标准的服务，促进新型生物药物开发。