南京招聘

主要职责：

？ 负责受试者数据库和信息管理

？ 日常管理预约受试者的随访

？ 研究者文件夹的建立和维护

？ 研究文件和药品或物品的接收，发放、保存、清点和归还

？ 研究数据的输入和核对

？ 协调CRA 与研究者的沟通

工作要求：
1．诚信，敬业，勤奋，踏实；
2．临床医学或药学相关专业毕业，在研究中心(医院)工作
3. 熟悉site 人际关系和工作流程；
4．较强的独立工作能力及团队合作精神

医院医生和护士兼职亦可！

Responsibilities:
-Management of subject database and information
-Daily management of subjects with appointment
-Creation and maintenance of investigator's folder
-Receival, distribution, preservation, counting and return of research documents or drugs/substance
-Input and verification of research data
-Coordinate communications between CRA and Investigator

Requirements:
-To be faithful, dutiful, diligent and steady
- Graduate of clinical medicine, pharmacy or related disciplines with prior experience in research centers (hospitals)
- Be familiar with the interpersonal relationship and workflow of site
-Be able to work both independently and as a team member

上海百试达医药科技有限公司是为国内外医药和医疗器材企业提供高质量临床研究专业服务的合同研究组织（CRO），是国内领先的医药研发服务外包承接机构。公司临床研究服务分布在药品、医疗器械、生物制品等领域，为客户提供专业化的技术解决方案和技术服务。

上海百试达业务范围包括临床试验的设计、组织、运作和管理，如I-IV 期药物临床试验和医疗器械临床试验项目的策划和筹备、方案撰写、基地筛选、临床监查服务、药物管理、数据管理和生物统计、研究报告撰写。公司还提供药品和医疗器械注册和医学咨询和代理、流行病学观察性研究、医药市场研究和研究者、CRA 和其他临床研究专业人员的培训等。

上海百试达拥有资深的专业研究团队，主要研究人员均具有外资制药企业药物研发部和临床研究部工作经验。具有国际化、标准化的业务运作流程和科学严谨的质量保证体系，谙熟国际多中心临床试验和国内各种类型临床试验项目的运作和管理。此外，百试达还在临床医学，临床药理学和生物统计领域拥有一大批专家网络资源，并通过高质量的各类人员和项目培训不断扩大这一网络，从而保证各类临床项目的快速和高质量的完成。

公司的合作客户包括知名跨国制药公司和医疗器械企业、国内研发型制药企业、医药科研院所以及专业学术团体等。
公司总部位于上海，在北京、广州、成都设立分支机构，服务范围覆盖全国多个中心城市和区域；在美国波士顿设有联络处和QA 办公室。

Bestudy are one of the leading contract research organizations (CRO) that provides high-quality clinical studies service for domestic and overseas pharmaceutical and medical device enterprises in the country. We provide professional technical solutions and services for our customers' clinical studies in the fields of medicine, medical device and biological products.

We are specializing in design, organization, operation and management of clinical trials, eg, planning, preparation, protocol writing, site selection and due diligence, clinical monitoring service, investigational product management, data management, bio-statistics and study report writing for phase I-IV drug and medical device clinical trial project. It also provides medicine and medical device registration and medical consulting and agent, epidemiological observational research, drug market research and the training of study professionals including investigators, study nurse, CRAs and other clinical trial staffs.
We have professional research team with a majority of members who worked years in R&D and clinical research departments of multinational pharmaceutical companies. With the world leading and standard business process and scientific quality assurance system, Bestudy has accumulated proficient experience in the operation and management of multicenter clinical trial projects and other clinical trial projects in China. In addition, we boast a wealth of expert resources in clinical medicine, clinical pharmacology and bio-statistics and try to further extend through personnel development program and project training to make sure various clinical projects are completed with speed and high quality.

We have built the partnership with multinational pharmaceutical and medical device enterprises, R&D-oriented pharmaceutical enterprises and pharmaceutical research institutes and academic societies.

Headquartered in Shanghai, we have subsidiaries in Beijing、Chengdu and Guangzhou with business operations in many central cities and regions across the country and opened international business and QA office in Boston, USA.