杭州招聘

岗位职责：

1. Independently be responsible for all activities of the clinical research, including clinical site selection, study initiation visits, training of on-site personnel, study close and trial monitoring with on-site audits of clinical data for accuracy and completeness, and clinical report preparation and presentation.独立负责临床试验中的所有环节，包括临床试验单位的选择，临床试验启动、人员培训、项目结题、临床监察，进一步负责临床数据准确性以及完整性，并且准备和获得临床试验报告。

2. Prepare study protocols, investigator manuals, site specific instruction manuals and design case report forms.准备临床试验相关的所有文档，包括临床方案、研究者手册、临床单位的操作指南以及病例报告表等。

3. Assist with the management of key study parameters, including documents, clinical research products, start-up activities, enrollment, data collection, etc..协助管理临床试验中的所有关键性因素，包括文档、临床试验所用产品、临床试验启动、病例入组、数据收集等。

4. Slove the problems or issues that could affect the results or timely completion of the trial. 解决所有可能会影响到临床试验结果或者临床试验结束时间的各种问题。

任职要求：

1. 工作经验：Minimum of 3 years experiences with In Vitro Diagnostic (IVD), especially in molecular diagnostics or immunodiagnostics. Having the working experience in the MCN company or local well-known company is preferred. 至少3年以上体外诊断试剂领域临床试验工作经验,尤其是分子诊断或者免疫学诊断相关领域的经验。具有跨国企业或者本土知名企业工作经验者优先。

2. 教育背景：Bachelor's Degree or above of Medical/Biological related major. Master degree is prefeered. 医学/生物学相关专业本科以上学历，研究生学历优先。

3.语言技能：Fluent Reading and Writing English; Communication: Highly developed interpersonal skills; Characters： Well organizing details of the project, and sensitive to details. Willing to travel. 熟练的英语阅读和写作能力；相熟的沟通能力；良好的细节管理能力。

4.技术能力：Clinical Research Skills: Organizing clinical trial of Medical Devices/IVD, being familiar with GCP and CFDA guidelines. Multi-tasks Management: Having experience on the multi-tasks management, have the capability to handle and drive more than 3 projects at the same time.临床试验技巧：组织过医疗器械/体外诊断试剂临床试验，熟悉GCP和CFDA的技术指南；多项目管理：拥有多项目管理经验，并且有能力协调和开展多个项目

EUROIMMUN was founded in September 1987 and today has its headquarters in Lübeck, Germany. EUROIMMUN produces reagents for medical laboratory diagnostics. In the foreground are test systems for the determination of various antibodies in patient serum in the diagnosis of autoimmune diseases, infectious diseases and allergies. The company is based on worldwide-patented state-of-the-art production methods and microanalysis techniques and is one of the world's leading manu¬facturers of medical laboratory diagnostics. The company’s reference laboratory is unequalled in the whole field of autoimmune diagnostics. It helps EUROIMMUN customers to secure their results. With their quality and standardization, EUROIMMUN products are capturing the leading position in the world.
EUROIMMUN embarked China in 1999. The Beijing office has now become the headquarters of EUROIMMUN Asia Pacific. The company sets high-standard research and production base in China and Singapore. Its sales teams cover most Asia-Pacific countries and regions such as China’s mainland, ChinaHong Kong, ChinaTaiwan, South Korea, Singapore and Thailand. With numerous global patents, state-of-the-art technology and clinical diagnostics techniques, the company wins high recognition from here and has become the leader of Asian market.

欧蒙医学实验诊断股份公司由德国吕贝克大学病理学教授Winfried Stöcker博士创建于1987年，是世界领先的医学诊断试剂及自动化仪器研发与生产的跨国企业。逾两千名员工服务于全球近200个国家及地区，其产品和服务惠及世界五大洲数万间实验室。欧蒙集团在自身免疫性疾病、感染性疾病、变态反应性疾病诊断领域拥有领先的诊断方案，在分子诊断及抗原检测等领域拥有先进的技术。同时，专业的欧蒙参考实验室为全球用户提供疑难样本的诊断和验证服务，由德国DAP（德国实验室认证机构）认证的欧蒙全球质量评价项目为广大客户提供全球实验室质量交流平台，助力客户加强实验室质量管理。
欧蒙医学诊断(中国)有限公司于1999年成立于北京，是欧蒙亚太集团总部。公司在中国、新加坡建立有先进的产品研发和生产基地，专业技术团队遍及中国各省市、中国香港、中国台湾、韩国、新加坡、泰国等亚太国家及地区。凭借提供高品质、全方位的医学诊断方案，秉承科技创新造就卓越品质，欧蒙诊断促进人类健康的企业宗旨，欧蒙的技术、产品与服务赢得了亚太地区客户的高度认可与信赖，成为医学诊断市场的领导者。