IHCRA
上海康德弘翼医学临床研究有限公司
- 公司规模:500-1000人
- 公司性质:合资
- 公司行业:制药/生物工程
职位信息
- 发布日期:2017-03-30
- 工作地点:北京-朝阳区
- 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 良好
- 职位月薪:6-8千/月
- 职位类别:临床研究员
职位描述
职位描述:
Performs investigator recruitment activities utilizing phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites.
Utilizes the Clinical Trial Management System (CTMS) to ensure investigator recruitment activities are accurately tracked.
Performs essential document collection, review, maintenance and close-out activities, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regulatory requirements and ICH/GCP guidelines.
Supports investigators and investigative staff in fulfilling obligations with regard to local submissions according to local regulatory and Institution Review Board (IRB)/Independent Ethics Committee (IEC) requirements.
Performs study tracking via CTMS or Sponsor designated system to ensure that the study files are current, accurate and complete.
Documents site and Sponsor contact and study interactions in a timely and professional manner.
Assists with resolution of investigational site/data queries. Liaises with project team members regarding study site issues. Provides quality review of the informed consent template.
Performs study duties in adherence to the protocol, Clinical Management Plan (CMP), study processes, ICH-GCP and any other requirements stipulated on the study.
Follows up with sites for trial invoices and ensures CTMS is accurately updated to allow the timely processing of Investigator Payments.
Performs other duties as assigned.
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Performs investigator recruitment activities utilizing phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites.
Utilizes the Clinical Trial Management System (CTMS) to ensure investigator recruitment activities are accurately tracked.
Performs essential document collection, review, maintenance and close-out activities, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regulatory requirements and ICH/GCP guidelines.
Supports investigators and investigative staff in fulfilling obligations with regard to local submissions according to local regulatory and Institution Review Board (IRB)/Independent Ethics Committee (IEC) requirements.
Performs study tracking via CTMS or Sponsor designated system to ensure that the study files are current, accurate and complete.
Documents site and Sponsor contact and study interactions in a timely and professional manner.
Assists with resolution of investigational site/data queries. Liaises with project team members regarding study site issues. Provides quality review of the informed consent template.
Performs study duties in adherence to the protocol, Clinical Management Plan (CMP), study processes, ICH-GCP and any other requirements stipulated on the study.
Follows up with sites for trial invoices and ensures CTMS is accurately updated to allow the timely processing of Investigator Payments.
Performs other duties as assigned.
职能类别: 临床研究员
关键字: IHCRA CRA 临床监察 CRC
公司介绍
康德弘翼(WuXi Clinical),是药明康德(WuXi AppTec)的一家全资子公司。始终致力为全球客户提供全方位的临床研究服务,包括药品、生物制品、医疗器械、体外诊断试剂等医药产品。从I期临床研究到最终申报注册,通过严格的质量控制体系和专业团队的丰富经验,帮助创新性,突破性医药产品尽快上市和造福患者。
康德弘翼立足中国,面向世界,以上海总部为中心,辐射全球制药公司、生物技术公司以及医疗器械公司。目前,公司实行中美联合运营,人员规模达850人,覆盖中美两地,全国30多个主要城市,在上海、北京、广州、武汉、成都、长沙、西安、沈阳和美国奥斯汀、圣地亚哥10个城市均设有办公室。公司团队与各研究中心建立了良好的合作关系,始终保持着紧密的业务交流,保证了项目能高效、高质地完成。
随着业务能力的不断提升,我们已将业务范围成功扩展到美国、欧盟和亚太地区的部分国家。2018年7月,药明康德成功收购位于德克萨斯州的一家美国临床研究机构并实现中美联合运营,2019年5月,再一次收购了位于圣地亚哥的临床研究服务公司Pharmapace,这让WuXi Clinical的规模再一次得到扩大,进一步完善和增强了我们全球一体化研发服务平台的综合实力,帮助全球创新合作伙伴更好、更快地开发医药产品。
康德弘翼立足中国,面向世界,以上海总部为中心,辐射全球制药公司、生物技术公司以及医疗器械公司。目前,公司实行中美联合运营,人员规模达850人,覆盖中美两地,全国30多个主要城市,在上海、北京、广州、武汉、成都、长沙、西安、沈阳和美国奥斯汀、圣地亚哥10个城市均设有办公室。公司团队与各研究中心建立了良好的合作关系,始终保持着紧密的业务交流,保证了项目能高效、高质地完成。
随着业务能力的不断提升,我们已将业务范围成功扩展到美国、欧盟和亚太地区的部分国家。2018年7月,药明康德成功收购位于德克萨斯州的一家美国临床研究机构并实现中美联合运营,2019年5月,再一次收购了位于圣地亚哥的临床研究服务公司Pharmapace,这让WuXi Clinical的规模再一次得到扩大,进一步完善和增强了我们全球一体化研发服务平台的综合实力,帮助全球创新合作伙伴更好、更快地开发医药产品。
联系方式
- 公司地址:上海市黄浦区淡水路299号SOHO复兴广场A幢801室 (邮编:200020)