Clinical Project Assistant
科锐国际人力资源（北京）有限公司
- 公司规模：1000-5000人
- 公司行业：专业服务(咨询、人力资源、财会)
职位信息
- 发布日期：2014-04-30
- 工作地点：上海
- 招聘人数：若干
- 语言要求：英语熟练
- 职位月薪：面议
- 职位类别：临床研究员
职位描述
JOB PURPOSE:
The main tasks of the Clinical Project Assistant (CPA) are the administrative support of the set-up, monitoring and reporting of clinical trials in conformity with Good Clinical Practice and Sanofi-Synthelabo’s internal Standard Operating Procedures in order to facilitate to a high extent the execution of the research projects.
ORGANIZATIONAL CONTEXT:
(See Organizational chart attached)
SUPERVISED RESOURCES:
(Sales, budget, headcount…)
KEY ACCOUNTABILITIES:
1. The efficient and accurate administrative processing of forms concerning data collection, medication and other materials with regard to clinical trials. Activities are based on the guidelines as described in Sanofi-Synthelabo’s Standard Operating Procedures.
2. Set up, manage and keep up-to-date the trial archives in accordance with the Sanofi-Synthelabo Standard Operating Procedures for filing of trial documents (among which the so-called “core file”) in such a way that any relevant information can be presented promptly during internal or external audits.
3. Be an internal focal point for the Clinical Research Associates and Clinical Research Physicians working on-site.
4. Communicate with external relations on a professional level.
JOB-HOLDER ENTRY REQUIREMENTS:
Education:
Experience & knowledge:
Good working knowledge of all relevant Standard Operating Procedures and guidelines with regard to Good Clinical Practice.
Core competencies:
- Excellent communicative skills and a professional attitude
- Common sense, efficiency and flexibility
- Has an eye for details
- Fluency in English, spoken and in writing
- Adequate knowledge of common softwares is required.
The main tasks of the Clinical Project Assistant (CPA) are the administrative support of the set-up, monitoring and reporting of clinical trials in conformity with Good Clinical Practice and Sanofi-Synthelabo’s internal Standard Operating Procedures in order to facilitate to a high extent the execution of the research projects.
ORGANIZATIONAL CONTEXT:
(See Organizational chart attached)
SUPERVISED RESOURCES:
(Sales, budget, headcount…)
KEY ACCOUNTABILITIES:
1. The efficient and accurate administrative processing of forms concerning data collection, medication and other materials with regard to clinical trials. Activities are based on the guidelines as described in Sanofi-Synthelabo’s Standard Operating Procedures.
2. Set up, manage and keep up-to-date the trial archives in accordance with the Sanofi-Synthelabo Standard Operating Procedures for filing of trial documents (among which the so-called “core file”) in such a way that any relevant information can be presented promptly during internal or external audits.
3. Be an internal focal point for the Clinical Research Associates and Clinical Research Physicians working on-site.
4. Communicate with external relations on a professional level.
JOB-HOLDER ENTRY REQUIREMENTS:
Education:
Experience & knowledge:
Good working knowledge of all relevant Standard Operating Procedures and guidelines with regard to Good Clinical Practice.
Core competencies:
- Excellent communicative skills and a professional attitude
- Common sense, efficiency and flexibility
- Has an eye for details
- Fluency in English, spoken and in writing
- Adequate knowledge of common softwares is required.
公司介绍
作为亚洲领先的招聘整体解决方案提供商，科锐国际人力资源有限公司成立于1996年，目前在大中华地区拥有12个直属分公司及34个重点城市分支机构，超过900名专业招聘人员。科锐国际致力于在17个细分行业与领域中为客户提供最优质的服务，以满足客户在所有层次的招聘需求。科锐国际的客户80%来自世界知名集团，20%来自国内上市公司、快速成长性企业及非赢利组织。在过去的一年中，科锐国际成功为企业推荐的长期雇员及派遣雇员总数超过万人，中高级专业职位及管理职位超过4500个。