• 招聘类型：社招
• 工作性质：全职
• 所属区域：北京 - CBD
• 直属部门：Clinical Operations

职位描述

• Delivery of clinical start-up component of assigned studies with accountability for time, cost and quality for assigned activities, which include, but not limited to,

o Investigator/Site identification, including conduct feasibility activity to identify investigators and conduct site visit to confirm qualification for the required study

o Prepare IRB submission

o Clinical trial site contract and budget negotiation, if required

o Prepare, submit regulatory documents to HGRAC and obtain approval for required study

• Assist in maintain and update company-level investigator database
• Establish, maintain and enhance relationship with key opinion investigators and sites
• Proactively identify potential issues and seek improvement. Take initiative for issue resolution within and outside start-up team. Coordinate the risk management process encompassing proactive risk identification, evaluation (probability and impact) and mitigation plans
• Perform other duties as assigned by management

任职条件

• Bachelor’s level degree or above in life sciences, pharmacy, nursing or medical
• Knowledgeable in the execution of clinical trials, understanding of GCP/ICH Guidelines and other applicable regulatory requirements
• At least 3 year of clinical research experience in the Pharmaceutical or CRO industry
• Self-motivation with the ability to work under pressure to meet deadlines
• Fluent in English (writing and speaking)

职位要求

• 学历要求：无
• 工作经验：无
• 外语要求：不需要

公司福利

• 五险一金 
• 晋升空间 
• 法定节假日