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[全国]西斯比亚(北京)医药技术研究有限责任公司

职位:临床协调员
发布时间:2024-10-18
工作地点:上海 北京 广州 南京 深圳 武汉 天津 成都 其它
信息来源:福建医科大学
职位类型:全职
专业标签:临床医学
职位描述

西斯比亚(北京)医药技术研究有限责任公司

临床协调员

1K-3K/月 全国 本科及以上

职位诱惑:岗前培训 交通补助 餐补 岗位晋升 带薪年假

发布时间:2024年10月18日

职位描述

岗位职责:

1、Knowledge of the protocols and through knowledge of the examinations and procedures in connection with the Study Nurse position as discussed in the protocols and in accordance with the study specific defined responsibility log.

2、Thorough knowledge of CCBR procedures and quality control regulations (relevant for the Study Nurse position), which forms the basis of performing clinical studies.

3、Knowledge of international/national regulations and instructions for performing clinical studies.

4、Perform in a professional, kind and efficient manner, when taking care of study participants.

5、Thorough knowledge to the content of the Study File and responsible for the document filling.

6、Have a good grasp of the Patient File.

7、Responsible for the content of the Patient File, general pages as well as study specific pages.

8、Responsible for coordination concerning eligibility in the study enrolment phase.

9、Update study staff members on current study procedures and other relevant information.

10、Make appointments with Sponsors representative for monitoring.

11、Always be updated on the current study status.

12、Thorough knowledge of the time schedule.

13、Handling of drug supplies. Handling of test results.

14、Last check of Patient Files and CRF’s.

15、To participate in and add information to planned clinic meetings.

16、To participate in education and training planned by CCBR.

17、To participate in arrangements planned by CCBR, with the purpose of nurturing the solidarity between individual demarcation groups and collaborating groups.

18、To participate in subject recruitment program/community out reach.

19、Participate in meetings arranged by Study Management Manager/GM; such as investigator meetings, initiation meetings etc.

岗位要求:

1、Knowledge of the protocols and through knowledge of the examinations and procedures in connection with the Study Nurse position as discussed in the protocols and in accordance with the study specific defined responsibility log.

2、Thorough knowledge of CCBR procedures and quality control regulations (relevant for the Study Nurse position), which forms the basis of performing clinical studies.

3、Knowledge of international/national regulations and instructions for performing clinical studies.

4、Perform in a professional, kind and efficient manner, when taking care of study participants.

5、Thorough knowledge to the content of the Study File and responsible for the document filling.

6、Have a good grasp of the Patient File.

7、Responsible for the content of the Patient File, general pages as well as study specific pages.

8、Responsible for coordination concerning eligibility in the study enrolment phase.

9、Update study staff members on current study procedures and other relevant information.

10、Make appointments with Sponsors representative for monitoring.

11、Always be updated on the current study status.

12、Thorough knowledge of the time schedule.

13、Handling of drug supplies. Handling of test results.

14、Last check of Patient Files and CRF’s.

15、To participate in and add information to planned clinic meetings.

16、To participate in education and training planned by CCBR.

17、To participate in arrangements planned by CCBR, with the purpose of nurturing the solidarity between individual demarcation groups and collaborating groups.

18、To participate in subject recruitment program/community out reach.

19、Participate in meetings arranged by Study Management Manager/GM; such as investigator meetings, initiation meetings etc.

投递说明:

招聘方式

人力资源招聘组:AES_CCBR_HR_China@

公司网址:pr***com[点击查看]

单位简介

CCBR—全球第一大SMO集团,1992年在丹麦成立。于2019年9月CCBR被全球最大的临床研究中心集团AES并购。AES目前在五大洲,25个国家,拥有180多家临床研究中心。CCBR一贯秉承质量为本的理念,提供一流的科学专业知识服务。

西斯比亚(北京)医药技术研究有限责任公司是CCBR在中国区的子公司,创办于2005年9月。西斯比亚(北京)是国际临床研究中心协会(SCRS)董事会成员、中国GCP联盟合作成员及中国SMO协作组第一届理事会成员。西斯比亚(北京)目前在中国拥有600多名CRC,覆盖全国近120个主要城市



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西斯比亚(北京)医药技术研究有限责任公司


领域:科学研究和技术服务业

规模:500-1000人

地址:北京市昌平区生命园路29号中关村生命科学园创新大厦C座一层101

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