临床研究助理-CTA(Clinical Trial Assistant)
上海法码康数据管理有限公司
- 公司规模:少于50人
- 公司性质:合资(非欧美)
- 公司行业:医疗/护理/卫生
职位信息
- 发布日期:2012-09-07
- 工作地点:北京
- 招聘人数:6
- 工作经验:一年以上
- 学历要求:本科
- 语言要求:英语良好
- 职位类别:临床研究员
职位描述
Responsibilities:
1.Assist Clinical Team Lead (CTL) and Clinical Research Associates (CRAs) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines;
2.Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for accuracy and completeness;
3.Assist CTLs with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information;
4.Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow;
5.Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation;
6.Provide administrative support to team members with clinical trial execution.
Requirements:
1.Bachelor degree or equivalent combination of education, training and experience.
2.Awareness of knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.
3.Knowledge of applicable protocol requirements as provided in company training;
4.Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint;
5.Strong written and verbal communication skills including good command of English language;
6.Attention to detail and accuracy in work;
1.Assist Clinical Team Lead (CTL) and Clinical Research Associates (CRAs) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines;
2.Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for accuracy and completeness;
3.Assist CTLs with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information;
4.Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow;
5.Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation;
6.Provide administrative support to team members with clinical trial execution.
Requirements:
1.Bachelor degree or equivalent combination of education, training and experience.
2.Awareness of knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.
3.Knowledge of applicable protocol requirements as provided in company training;
4.Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint;
5.Strong written and verbal communication skills including good command of English language;
6.Attention to detail and accuracy in work;
公司介绍
法码康概况:
法码康是一家医药研发合同研究组织(CRO),其团队成员来自全球领先的制药企业及CRO,凭借对行业的热情和执着,以及丰富的药品研发、管理及执行经验,不断为客户提供高品质的服务。同时法码康还是一家了解客户真正需求的医药研发外包服务提供商。我们在中国、澳大利亚和比利时,都设有办事处,并在美国、日本和其它亚洲国家都有战略合作伙伴。
法码康提供的服务:
作为一个深知客户需求的医药研发外包服务提供商,法码康为制药企业、 生物技术企业、医疗器械企业及医疗保健公司在研发领域提供外包服务,特别是在临床试验、注册事务、药物安全、质量监控、研究药物存储/处理/发放、生物统计及数据管理/统计/报告撰写等领域有所专攻。法码康凭借在医药行业十多年的经验以及深刻的认知、对行业的热情和服务精神,我们的服务将为您的产品增值添彩,并满足您对高质量和高效率的需求。
法码康拥有具备多年亚太地区临床研究工作经验的人员,依据完善的国际标准操作流程,为中国、澳大利亚与亚洲其它地区的客户提供研发服务。
我们的愿景:
法码康致力于成为亚太地区领先的医药研发外包服务提供商。
对客户的利益:
以最佳的研发方案确保产品提前上市,以最高质量的数据提升产品上市效果,令客户及管理层和股东满意。
公司网站:www.pharmacons.com
法码康是一家医药研发合同研究组织(CRO),其团队成员来自全球领先的制药企业及CRO,凭借对行业的热情和执着,以及丰富的药品研发、管理及执行经验,不断为客户提供高品质的服务。同时法码康还是一家了解客户真正需求的医药研发外包服务提供商。我们在中国、澳大利亚和比利时,都设有办事处,并在美国、日本和其它亚洲国家都有战略合作伙伴。
法码康提供的服务:
作为一个深知客户需求的医药研发外包服务提供商,法码康为制药企业、 生物技术企业、医疗器械企业及医疗保健公司在研发领域提供外包服务,特别是在临床试验、注册事务、药物安全、质量监控、研究药物存储/处理/发放、生物统计及数据管理/统计/报告撰写等领域有所专攻。法码康凭借在医药行业十多年的经验以及深刻的认知、对行业的热情和服务精神,我们的服务将为您的产品增值添彩,并满足您对高质量和高效率的需求。
法码康拥有具备多年亚太地区临床研究工作经验的人员,依据完善的国际标准操作流程,为中国、澳大利亚与亚洲其它地区的客户提供研发服务。
我们的愿景:
法码康致力于成为亚太地区领先的医药研发外包服务提供商。
对客户的利益:
以最佳的研发方案确保产品提前上市,以最高质量的数据提升产品上市效果,令客户及管理层和股东满意。
公司网站:www.pharmacons.com
联系方式
- 公司地址:上海市长宁区淮海西路432号6楼B座
- 邮政编码:200052
- 联系人:Sunny Wang
- 传真:(021)52308089
- 电话:(021)51863638