更新于 12月18日

Clinical Study Lead

2.4万-3万·14薪
  • 北京朝阳区
  • 3-5年
  • 硕士
  • 全职
  • 招1人

职位描述

临床试验生物工程临床项目管理临床方案
Position description:
1. Responsible for trial design, planning (timeline and budget) and accountable for clinical study projects in China territory of Qiagen organization by coordinating with activities and stakeholders internally and externally.
2. Ensure compliance to SOPs, GCP policy, and relevant CFDA regulations in the operation of clinical study.
3. Responsible for tracking of timeline and budget, ensuring complete trial in a timely manner within budget, and raise up potential issues timely, setup internal and external communications for correction, trouble shooting, and prevention plan.
4. Draft and implement all study associated documentation including ethical application, CFDA files of trial, study protocols, contracts, site files, audit reports, and study reports.
5. Review all source documentation, monitor reports, site record, and data for accuracy and ensure timely submission and safe storage of all documentation.
6. Execute site survey/selection, guide lab preparation, instrument/reagent setup, kick-off meeting/training, logistic of consumables supply and inventory in line with regulations.
7. Lead CRA/CRC (internal and external) to plan site monitoring, and ensure good monitoring quality in terms of documentation, enrollment progress, data records. Lead data specialist for database design, database implementation on site, integrity check planning, and statistic strategy.
8. Coordinate communications with investigators, and participate discussions with CFDA relevant reviewers / guideline drafter if necessary
Hiring requirement/preference:
1. At least 4 years IVD clinical trial related experiences, Pharma trial experiences could be considered as well, better clinical project management roles.
2. Strong and solid IVD or bio-tech knowledge, medical or clinical lab related backgrounds preferred.
3. Proficiency of English oral communication, and technical reading and writing.
4. Excellent knowledge in CFDA regulation, ISO international standards, and relevant clinical trial guidance.
5. Strong ability in inter-personal skill, project management skill, problem-solving mindset

工作地点

太阳宫大厦1103

职位发布者

梁晓霞/人事经理

三日内活跃
立即沟通
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QIAGEN是一家专业化致力于生物分子样品制备解决方案的跨国经营企业,总部位于德国。1984年,QIAGEN在德国成立,1996年在美国纽约纳斯达克上市。QIAGEN在全球有亚太、日本、北美、欧洲四个地区总部,有19个分公司,有近3,000雇员,有超过500个的产品,有超过40万的用户,拥有409个已被批准的专利,有300多种专利正在申请之中。是在生命科学研究、应用检测和临床诊断等领域的行业巨头。作为分子检测技术领袖,生物分子样品制备方案的全球主要供应商,QIAGEN-凯杰生物科技可谓名声赫赫,是大家听得比较多的名字。许多生物科学家们都对QIAGEN推崇备致,交口称赞QIAGEN的生物分子分离纯化制备技术,无一例外的声称自己取得的科研成果都得益于QIAGEN的产品和技术。
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