CRA I/II 临床监查员
精鼎医药研究开发（上海）有限公司
- 公司规模：10000人以上
- 公司性质：外资(欧美)
- 公司行业：制药/生物工程
职位信息
- 发布日期：2017-04-15
- 工作地点：长春
- 招聘人数：若干人
- 工作经验：1年经验
- 学历要求：本科
- 语言要求：英语 精通
- 职位月薪：4000-10000/月
- 职位类别：临床协调员
职位描述
职位描述：
现招聘 长春home based CRA，至少1年CRO行业工作经验，有意者请发送简历至tony.feng艾特parexel.com
*Job Posting Description
PAREXEL provides monitors with world class technology, training resources, and limited protocol load. You will also be rewarded for your hard work through our CRA bonus incentive program and career advancement opportunities.
Your Key Accountabilities:
?Perform all clinical monitoring/site management activities for assigned projects in accordance with PAREXEL's standard operating procedures
?Act as PAREXEL's direct contact with assigned clinical sites, and use judgment to assess and ensure overall integrity of study implementation, as well as adherence to study protocol
?Conduct qualification visits (QV), site initiation visits (SIV) and monitoring visits (MV) at assigned clinical sites
?Build strong working relationships with investigators and site staff
?Manage clinical monitoring activities, including:
？Arranging on-site visits and logistics
？Establishment of a site recruitment plan in collaboration with site staff during QV
？Monitoring completeness and quality of Regulatory Documentation
？Performing site documentation verification
？Data collection and drug accountability in accordance with ICH GCP guideline
？Monitoring patient safety on-site and addressing any violations in a timely manner
*Job Posting Qualifications
Your Skillset:
?Educated to degree level (biological science, pharmacy or other health related discipline)
?Strong written and verbal communication skills in local language
Our Offer:
We offer you a fascinating and diversified insight into PAREXEL and an exciting journey through the world of clinical research.
You can expect to work with a successful, highly-qualified and dynamic team as you develop your individual scientific profile. You can also look forward to a flexible working environment and a pleasant atmosphere.
If you are ready to join PAREXEL’s Journey, please apply!
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现招聘 长春home based CRA，至少1年CRO行业工作经验，有意者请发送简历至tony.feng艾特parexel.com
*Job Posting Description
PAREXEL provides monitors with world class technology, training resources, and limited protocol load. You will also be rewarded for your hard work through our CRA bonus incentive program and career advancement opportunities.
Your Key Accountabilities:
?Perform all clinical monitoring/site management activities for assigned projects in accordance with PAREXEL's standard operating procedures
?Act as PAREXEL's direct contact with assigned clinical sites, and use judgment to assess and ensure overall integrity of study implementation, as well as adherence to study protocol
?Conduct qualification visits (QV), site initiation visits (SIV) and monitoring visits (MV) at assigned clinical sites
?Build strong working relationships with investigators and site staff
?Manage clinical monitoring activities, including:
？Arranging on-site visits and logistics
？Establishment of a site recruitment plan in collaboration with site staff during QV
？Monitoring completeness and quality of Regulatory Documentation
？Performing site documentation verification
？Data collection and drug accountability in accordance with ICH GCP guideline
？Monitoring patient safety on-site and addressing any violations in a timely manner
*Job Posting Qualifications
Your Skillset:
?Educated to degree level (biological science, pharmacy or other health related discipline)
?Strong written and verbal communication skills in local language
Our Offer:
We offer you a fascinating and diversified insight into PAREXEL and an exciting journey through the world of clinical research.
You can expect to work with a successful, highly-qualified and dynamic team as you develop your individual scientific profile. You can also look forward to a flexible working environment and a pleasant atmosphere.
If you are ready to join PAREXEL’s Journey, please apply!
职能类别： 临床协调员
关键字： CRA CRC 临床 监查员 CRO
公司介绍
精鼎医药（Parexel International）是全球领先的药物研究合同委托机构（CRO），总部位于美国生物医药圣地马萨诸塞州的波士顿附近，在世界各地拥有71个办事处，约17,600 名员工，为超过100个国家的客户提供服务。
精鼎医药成立于1982年，在三十多年的历程中，一直致力于发展成为全球生物制药和医疗器械行业首屈一指的新型医学疗法开发和商业化服务供应商，并且取得了卓越成果。目前，我们能够提供全世界CRO领域全面的新药临床阶段研发服务，服务内容包括新药开发策略的拟定与计划、国际临床试验规划执行及整合、临床试验的监测、临床试验数据处理、临床研究统计分析、临床试验总结及统计报告、临床试验稽核服务、临床试验供应和物流服务、临床电子数据采集、临床医学信息管理系统、新药查验登记事务和国际临床试验相关法规咨询等。
将我们的全球法规监管专业经验、I-IV期临床研究服务、整合的电子化临床技术能力和商业化服务结合在一起的一体化解决方案，可帮助我们的客户更加顺畅、经济和高效的推动整个研发历程。
精鼎医药成立于1982年，在三十多年的历程中，一直致力于发展成为全球生物制药和医疗器械行业首屈一指的新型医学疗法开发和商业化服务供应商，并且取得了卓越成果。目前，我们能够提供全世界CRO领域全面的新药临床阶段研发服务，服务内容包括新药开发策略的拟定与计划、国际临床试验规划执行及整合、临床试验的监测、临床试验数据处理、临床研究统计分析、临床试验总结及统计报告、临床试验稽核服务、临床试验供应和物流服务、临床电子数据采集、临床医学信息管理系统、新药查验登记事务和国际临床试验相关法规咨询等。
将我们的全球法规监管专业经验、I-IV期临床研究服务、整合的电子化临床技术能力和商业化服务结合在一起的一体化解决方案，可帮助我们的客户更加顺畅、经济和高效的推动整个研发历程。
联系方式
- Email：tony.feng@parexel.com
- 公司地址：上海市浦东新区商城路506号新梅联合广场B座9层 (邮编：200120)