职位详情

CTA 临床部门助理(英语方向)

面议

上海浦东新区 经验不限 本科
缔脉生物医药科技(上海)有限公司

医药企业 其他 规模不详

职位描述
  • 节日福利
  • 五险一金
  • 带薪年假
Position Summary
Provide administrative, technical and logistical support to clinicaltrial projects and activities.

Key Responsibilities
Documents translation and format adjusting.
Arrange meeting logistics, such as book travel, event organization, etc.Support study team for EC/ HGRAC submission.
Coordinate on study documents filing.
Support meeting minutes, tracking and documentation

Education and Key Competency Requirement
Bachelor degree or above, English/ Administrative/ medical /pharmaceutical / life science background will be a plus.
Customer and service orientation.
Good teamwork and collaboration, effective communication (written andoral in both Chinese and English).
Effective computer and office skills to be able to use relevant systemand tools

职位简介
支持临床试验支持团队提供行政、技术和后勤的工作。

主要责任
试验相关资料的翻译及排版。
会议室预定及会前准备工作。
协助试验团队准备伦理/遗传办递交资料。
试验文件整理及存档。
协助记录会议纪要。
预定差旅机票及酒店。


教育和资质要求
本科或以上学历,相关医药专业优先,其他专业也可,至少两年相关工作经验。
有较强的团队合作精神。
善于与他人沟通,有良好的服务意识以及较强的应变能力。
熟悉办公软件如:WORD, PPT, EXCEL等。
英语水平良好,有较强的读写能力,大学英语四级或以上。

企业介绍:
缔脉生物医药科技(上海)有限公司是一家临床合同研究组织(CRO),旨在为中国及全球生物医药公司和医疗器械公司提供高水准全方位的服务,包括为客户就临床开发的各个方面及产品注册申报出谋划策,也提供与临床试验相关的各种支持。致力于提高研发产品的成功率。
dMed Biopharmaceutical Company Limited is a clinical Contract ResearchOrganization (CRO), providing high-end services to innovativebiopharmaceutical and medical device companies. dMed is committed toincreasing the probability of success of R&D products. Its servicesinclude Consulting, Clinical Operations, Biostatistics &Programming, Data Management, Pharmacovigilance, Clinical Science &Medical Affairs, Quality Assurance, Regulatory Affairs & Strategy.

我们的团队Our Team

• 团队管理成员全部来自全球一流生物医药企业,或跨国临床研究外包服务企业的高级管理人员
From executive and management team of global leading biopharmaceuticalcompanies or multinational Contract Research Organizations
•在各期临床试验及各类疾病领域拥有广泛经验,熟悉中国,美国,欧盟,日本等各地临床试验法规
Expertise in various therapeutic areas and all phases of clinicaltrials, familiar with clinical trial regulations in China, US, EU, Japanand other markets
• 拥有高度责任感为客户服务,值得信赖的专业团队
Trustworthy and Professional team with strong sense of accountability toserve our clients

服务对象及主营业务Our Clients and Services

• Provide service for domestic biopharmaceutical and medical devicecompanies and small and medium-sized biopharmaceutical and medicaldevice companies interested in China market End-to-End Servicesincluding Clinical Trial design and conduct, clinical trial dataAnalysis and Report, Regulatory submission, Systems support, FunctionalServices, comprehensive Consultation Services
• Provide service for multinational biopharmaceutical and medical devicecompanies (In China for China & In China for Global), such asStatistics, Data Management, Programming, Medical Writing,Pharmacovigilance and Risk Management, Regulatory documentation supportand operations, Quality Assurance & Audit

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详情请见公司********.dmedglobal.com
职位要求
  • 专业要求: 药学,英语
  • 最低学历: 本科
  • 工作年限: 经验不限
  • 职称要求: 初级
  • 英语等级: 英语六级
  • 招聘人数: 2
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