北京招聘

职位描述：
行政人事助理岗位职责:
　　1、负责招聘工作，应聘人员的预约，接待及面试;
　　2、员工入职手续办理，员工劳动合同的签订、续签与管理;
　　3、公司内部员工档案的建立与管理;
　　4、负责与其他部门的协调工作，做好信息的上传下达;
　　5、负责公司各部门的行政后勤类相关工作;
　　6、负责考勤及工资绩效的核算;
　　7、负责部门一些日常行政事务，配合上级做好行政人事方面的工作;
　　8、负责制定、监督及执行企业管理规章制度、行政人事管理制度以及工作流程、绩效考核制度;
　　9、负责组织企业文化建设工作，包括公司庆典、年会安排、会务组织、文体活动安排等;
　　10、协助上级制定各部门岗位职责说明书，报批后监督并执行;
　　11、协助上级制定员工培训计划，包括新员工培训以及所有员工的培训计划;
　　2、负责对新员工进行企业制度与文化的培训工作，建立企业形象;
　　13、负责协助各部门进行人员招聘工作，包括招聘流程、面试记录与筛选推荐等;
　　14、制定岗位晋升、下调策略，报批通过后加以监督执行;
　　15、制定薪酬上调、下调策略，报批通过后加以监督执行;
　　16、负责离职员工的善后处理工作，包括办公用品、钥匙、出勤核算、离职证明、合同解除等;
　　17、负责管理劳动合同、保密协议、房屋租赁协议以及各类人事行政文档;
　　18、协助各部门做好节假日期间工作安排，包括值班安排、检查门窗、关闭电源电脑等工作;
　　19、负责企业资产配置(包括办公设备、办公用品)的管理工作，包括清点、维护、登记等;
　　20、其他突发事件的处理。任职资格 举报 分享

北京比中生物医学科技有限公司是一家比利时背景的临床研究CRO（Contract Research Organization）公司。 欧盟首都比利时在生物医药研究与开发领域雄居世界领先地位,站在巨人的肩膀上的比中生物是一家国际化领先的临床研究技术服务机构。

比中生物医学科技有限公司提供国内外新药、医疗器械、生物制品、化妆品与保健品等产品I期至IV期临床试验相关的一系列专业技术服务， 从试验方案设计到向药监局提交临床总结报告并答辩的整个过程。 包括产品注册、研究方案设计、随机化、项目管理、临床监查稽查、 数据管理、统计分析、临床研究报告撰写、协助研究者发表SCI文章、市场调研和产品开发战略咨询、临床试验各阶段技术人员外派等。

我们致力于为我国学术界和产业界的生物医药研究与开发提供专业的符合国际标准的临床试验全程服务, 特别是在国内CRO公司技术较薄弱的数据管理，生物统计，医学写作，产品海外注册等方面；我们的努力，将为推动我国创新药物临床试验国际化进程贡献一份力量。
BC-BIOSTAT is a CRO (Contract Research Organization) with Belgium and China joint venture. We provide a range of professional full services, from protocol design until the product registration, for medicines, medical devices, biological products, health care products, diagnostic reagents, and cosmetics.
We provide full services including Product Registration, Protocol Design, Randomization (IVRS/IWRS), Clinical Audit and Inspection (CRA) services for clinical trials from Phase I to Phase IV, Data Management (EDC system), Statistical Analysis & Report (SAR), Clinical Study Report (CSR), Translation, article publication on SCI journals, presentation to the CFDA experts, and so on.
Our team brings together the world-class biostatistics and data management experts (Prof. Geert Molenberghs & Prof. Emmanuel Lesaffre). The company commits to provide services in professional bio-pharmaceutical research, and to develop Chinese medical academia and industry to meet international standards of clinical trials, especially data management and biostatistics services.
Since we started our business in China, we have established a very good cooperative relationship with pharmaceutical companies, clinical trial bases which are approved as clinical trials qualified hospitals by CFDA and the regulatory authorities of the Pharmaceutical Affairs. We have all kinds of professional and technical persons. We employ the national drug review experts, the base directors and the clinical expert council which has extensive influence in new drug clinical research.
We can act as an agent to help Chinese pharmacies enter into the European markets, and for international pharmacies to bring their products into China. BC-BIOSTAT conducts the product registration and the clinical trials for the registration in Europe and in China.
 
Our Mission：Experts, Experience, Execution, and Exceptional Results. It’s a powerful combination that delivers the results you demand.
Our Vision：Our vision is to be recognized by clients as the undisputed leader in China CRO industry by providing innovative, quality professional expertise, market intelligence and partnering solutions to meet the dynamic needs of the pharmaceutical, biotechnology and healthcare industries. Our hallmark shall to be great people, high quality data, flexible processes, and on-time delivery on low cost. To achieve it, we strive to operate within the industry’s highest medical, scientific, and regulatory standards, with uncompromising integrity and ethics, and respect for employees, clinical trial participants, investigators, suppliers, and the community.
Our Value：CUSTOMIZATION QUALITY INTEGRITY TEAMWORK KNOWLEDGE EXCELLENCE