高级临床研究专员
北京普林格医药技术有限公司
- 公司规模:少于50人
- 公司行业:医疗/护理/卫生 制药/生物工程
职位信息
- 发布日期:2013-09-04
- 工作地点:北京
- 招聘人数:若干
- 工作经验:二年以上
- 学历要求:本科
- 职位类别:临床研究员
职位描述
Job description
- Conduct project management for specific clinical trial as project leader
- Conduct site monitoring as monitor
- Ensure accordance with the approved protocol, SOPs and ICH-GCP
- Prepare protocol and clinical study report
- Design CRF and prepare essential documents
- Develop close connection with investigator and study site
- Frequent traveling required
职位描述:
- 作为项目经理负责临床试验的项目管理;
- 作为监查员执行研究中心监查;
- 确保临床试验项目按照方案、SOP和ICH-GCP实施;
- 准备临床研究方案和临床研究总结报告;
- 设计CRF、准备必须文件资料;
- 与研究者和研究中心保持良好的合作关系;
- 经常出差。
Qualification
- B.S. or higher degree on Medical / Pharmaceutical science
- At least 2 year relevant working experience
- Previous experience in international pharmaceutical company or CRO would be a plus
- Excellent site monitoring and site management skills
- Good problem solving and project management skills
- Excellent English communication skill
- Sufficient computer skills on Microsoft Office
任职要求
- 临床医学/药学专业本科或以上学历;
- 2年以上相关工作经验;
- 有外企制药企业或CRO公司工作经验者优先考虑;
- 优秀的研究中心监查和管理能力;
- 具有独立的解决问题和项目管理技能;
- 良好的英文交流技能;
- 熟练使用计算机及办公软件。
- Conduct project management for specific clinical trial as project leader
- Conduct site monitoring as monitor
- Ensure accordance with the approved protocol, SOPs and ICH-GCP
- Prepare protocol and clinical study report
- Design CRF and prepare essential documents
- Develop close connection with investigator and study site
- Frequent traveling required
职位描述:
- 作为项目经理负责临床试验的项目管理;
- 作为监查员执行研究中心监查;
- 确保临床试验项目按照方案、SOP和ICH-GCP实施;
- 准备临床研究方案和临床研究总结报告;
- 设计CRF、准备必须文件资料;
- 与研究者和研究中心保持良好的合作关系;
- 经常出差。
Qualification
- B.S. or higher degree on Medical / Pharmaceutical science
- At least 2 year relevant working experience
- Previous experience in international pharmaceutical company or CRO would be a plus
- Excellent site monitoring and site management skills
- Good problem solving and project management skills
- Excellent English communication skill
- Sufficient computer skills on Microsoft Office
任职要求
- 临床医学/药学专业本科或以上学历;
- 2年以上相关工作经验;
- 有外企制药企业或CRO公司工作经验者优先考虑;
- 优秀的研究中心监查和管理能力;
- 具有独立的解决问题和项目管理技能;
- 良好的英文交流技能;
- 熟练使用计算机及办公软件。
公司介绍
Prolink Pharma., Ltd.
Prolink (Prolink Pharma., Ltd.), established in April, 2003 in China, is a professional service provider (CRO, Contract Research Organization) for international pharmaceutical companies and innovative pharmaceutical units. Our services include pre-clinical research, pharmaceutical product registration, clinical study, and consulting. This is a special unit with high standard and quality, where you will be able to learn and really grasp the professional skill by hard work. Currently, Inspected by CFDA in May 2017, our term become the only one praised by CFDI inspector group for professional knowledge and responsibility since 722 storm in 2015.
Now we have several positions openings in several cities in China, interested candidates please send your CV in both English and Chinese to us by Email: hr@prolink-pharma.com (only Word format is available.)
Address: Suite 1301, Yi 5 Building, No.108 North 4th Ring Road East,
ChaoYang District, Beijing 100029, P.R.China
北京普林格医药技术有限公司
北京普林格医药技术有限公司(Prolink Pharma., Ltd.)成立于2003年04月,是一家为国际制药企业以及创新医疗产品研发机构提供专业技术服务的实体公司(合同研究组织,CRO),服务范围涵盖临床前研究、产品注册、临床研究、专业技术咨询服务等,多年来我们奉行高标准、高质量原则,在行业内是一个非常特殊的团队,在这里你通过努力能够真正学习并掌握专业技术。2017年05月我们负责的项目接受CFDA视察(药物临床试验数据核查),成为自722风暴(2015年)以来唯一受到CFDI现场表扬的团队。
目前在国内几个城市招聘临床研究人员,欢迎有兴趣的同行发送中英文简历(Word格式)至hr@prolink-pharma.com 。
公司地址:北京市朝阳区北四环东路108号乙5号楼1301室(邮编:100029)
招聘职位:
Clinical Research Associate (CRA)/ 临床研究专员
Prolink (Prolink Pharma., Ltd.), established in April, 2003 in China, is a professional service provider (CRO, Contract Research Organization) for international pharmaceutical companies and innovative pharmaceutical units. Our services include pre-clinical research, pharmaceutical product registration, clinical study, and consulting. This is a special unit with high standard and quality, where you will be able to learn and really grasp the professional skill by hard work. Currently, Inspected by CFDA in May 2017, our term become the only one praised by CFDI inspector group for professional knowledge and responsibility since 722 storm in 2015.
Now we have several positions openings in several cities in China, interested candidates please send your CV in both English and Chinese to us by Email: hr@prolink-pharma.com (only Word format is available.)
Address: Suite 1301, Yi 5 Building, No.108 North 4th Ring Road East,
ChaoYang District, Beijing 100029, P.R.China
北京普林格医药技术有限公司
北京普林格医药技术有限公司(Prolink Pharma., Ltd.)成立于2003年04月,是一家为国际制药企业以及创新医疗产品研发机构提供专业技术服务的实体公司(合同研究组织,CRO),服务范围涵盖临床前研究、产品注册、临床研究、专业技术咨询服务等,多年来我们奉行高标准、高质量原则,在行业内是一个非常特殊的团队,在这里你通过努力能够真正学习并掌握专业技术。2017年05月我们负责的项目接受CFDA视察(药物临床试验数据核查),成为自722风暴(2015年)以来唯一受到CFDI现场表扬的团队。
目前在国内几个城市招聘临床研究人员,欢迎有兴趣的同行发送中英文简历(Word格式)至hr@prolink-pharma.com 。
公司地址:北京市朝阳区北四环东路108号乙5号楼1301室(邮编:100029)
招聘职位:
Clinical Research Associate (CRA)/ 临床研究专员
联系方式
- Email:hr@prolink-pharma.com
- 公司地址:上班地址:北京市朝阳区北四环东路108号乙5号楼1301室