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Clinical Quality Support and Training Specialist | [查看更多类似职位] |
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工作地点 |
北京 |
发布日期 |
2008-05-02 |
工作年限 |
1年经验 |
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薪水范围 |
面议 | 学历要求 | 本科 |
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| 职位描述 |
职位类别： 生物/制药/医疗器械 工作地点： 北京 发布日期： 2008-02-27 工作经验： 1-3年 最低学历： 本科 管理经验： 否 工作性质： 全职 招聘人数： 若干 职位描述/要求： Location : Beijing Main Tasks: Familiar with ICH GCP, China GCP and company"s SOPs. Conduct GCP/SOP compliance check for local and CDP trials. Maintain and follow up action plan. Work as the coordinator to be involved in CQA audit conducted by HQ and help to complete action plan. Perform co-monitoring activities to ongoing trials. Implement Qua li ty Activity Plan (QAP) for c li nical trial function every year. Involve in global SOP review procedure, and give comments accordingly. Comparing with QBIQ SOPs, make gap analysis for local SOPs. Draft and update Local SOPs. Check QBIQ document li st according to SOP matrix regularly. Support to SOP training workshop, maintain group training records. Support to c li nical staffs training for the GCP, SOP and related clinical research regulations. Support to GCP training for external customer, as per required. Qualifications: Bachelor"s degree or above of Medical Science. 2-3 years working experience in clinical trials operation area. Working experience in qua li ty area. Fluency English on both written&verbal. 联系方式： 北京建国门外大街1号 国贸大厦2座31层， 诺和诺德（中国）制药有限公司 人力资源部收 (请在信封及简历上注明应聘职位) 邮编：100004， 传真: 010-65056668， E-mail: recruit@novonordisk.com (不可带附件) 请注明您所要申请的职位名称。 请注明您的户口所在地。 请您在应聘材料上标明，此职位的信息来源于zhaopin.com. .
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