更新于 4月23日
职位描述
临床试验中心管理CRO
Job Description
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.
The scope of responsibilities will include:
- Maintenance of databases and tracking systems
- Work with large amount of documents, including their compiling, procurement, processing, translation and filing
- Communication with company departments and external parties
- Communication point for investigative sites participating in the clinical research projects
- Coordination of site-specific query resolution, project training and access to vendor-related systems for site teams
- Receiving and routing all mails and incoming calls
- Assistance with meeting arrangements
- Preparation of draft agendas and minutes of project meetings
The scope of responsibilities will include:
- Maintenance of databases and tracking systems
- Work with large amount of documents, including their compiling, procurement, processing, translation and filing
- Communication with company departments and external parties
- Communication point for investigative sites participating in the clinical research projects
- Coordination of site-specific query resolution, project training and access to vendor-related systems for site teams
- Receiving and routing all mails and incoming calls
- Assistance with meeting arrangements
- Preparation of draft agendas and minutes of project meetings
Qualifications
- Bachelor Degree (Life Sciences)
- Prior administrative experience in Clinical Research / CRO environment, preferably in an international setting
- Full working proficiency English
- Proficiency in standard MS Office applications (Word, Excel and PowerPoint)
- Good organizational and planning skills, problem-solving abilities, flexibility
- Detail-oriented, able to multi-task and work effectively in a fast-paced environment
- Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects
- Prior administrative experience in Clinical Research / CRO environment, preferably in an international setting
- Full working proficiency English
- Proficiency in standard MS Office applications (Word, Excel and PowerPoint)
- Good organizational and planning skills, problem-solving abilities, flexibility
- Detail-oriented, able to multi-task and work effectively in a fast-paced environment
- Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects
Additional information
As a privately owned mid-size CRO, we are constantly growing, offering plenty of opportunities for personal and professional growth. With no investors to please, our management focuses on company culture and operational delivery over quarter-to-quarter profitability.
Make the right call and take your career to a whole new level. Join a company that focuses on its people and invests in their professional development and success.
Make the right call and take your career to a whole new level. Join a company that focuses on its people and invests in their professional development and success.
工作地点
朝阳区北京国贸大厦16号楼23层2357室
公司信息
辟埃赛医药科技(上海)有限公司
不需要融资 · 20-99人 · 医药研发/生产外包（CXO）
已审核
公司介绍
PSI is a leading full-service global Contract Research Organization providing a wide range of clinical trial services to the pharmaceutical and biotechnology industry, mainly for the development of clinical drugs. PSI has 2,200+ employees and 40+ affiliates in Europe, North and South America, Asia Pacific and South Africa. PSI是一家提供全方位服务的全球临床试验项目承包商，为制药和生物技术行业提供广泛的临床试验服务，以帮助临床药物的开发。PSI在欧洲、北美和南美、亚太和南非拥有2200多名员工和40多家分支机构。
工商信息
企业名称 辟埃赛医药科技（上海）有限公司
企业类型 有限责任公司（外国法人独资）
法人代表 Angelika Ruf
经营状态 存续
成立时间 2019-02-28
注册资本 20万瑞士法郎
认证资质
营业执照信息