更新于 2月11日
职位描述
临床试验
Company Description
PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
In this role you will streamline activities of project teams in China and ensure consistency of Clinical Operations processes across regions. You will ensure meeting study milestones by project teams on a country level, report study progress to clients and global stakeholders.
The scope of responsibilities will include:
- Manage clinical project timelines, milestones, schedules and updates during all project stages.
- Report project status updates and progress for a designated region; participate in Projects Review Meetings.
- Ensures consistency of all study processes across regions and identify regional differences.
- Communicate with Global Project Managers and clients.
- Manage project teams in the region, including team building, quality compliance, training and and monitoring of daily activities.
- Be a point of contact for contractors and third party vendors.
- Contribute to the development and update of project planning documents, essential documents, and project instructions.
- Oversee maintenance of study-specific and corporate tracking systems.
- Might be involved in regional project oversight for APAC.
Qualifications
- MPharm, RN or university/college degree in Life Sciences or an equivalent combination of education, training and experience
- Minimum 8 years’ site monitoring experience in China
- At least 2 years’ experience as Lead Monitor
- Experience supervising clinical project activities and leading clinical project teams
- Experience in oncology, gastroenterology, infectious diseases, autoimmune diseases, or any rare disease indication is preferable
- Communication, presentation, and customer-service skills
- Team building, leadership and organizational skills
- Full working proficiency in English and Chinese
- Proficiency in MS Office applications, including MS Project
PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
In this role you will streamline activities of project teams in China and ensure consistency of Clinical Operations processes across regions. You will ensure meeting study milestones by project teams on a country level, report study progress to clients and global stakeholders.
The scope of responsibilities will include:
- Manage clinical project timelines, milestones, schedules and updates during all project stages.
- Report project status updates and progress for a designated region; participate in Projects Review Meetings.
- Ensures consistency of all study processes across regions and identify regional differences.
- Communicate with Global Project Managers and clients.
- Manage project teams in the region, including team building, quality compliance, training and and monitoring of daily activities.
- Be a point of contact for contractors and third party vendors.
- Contribute to the development and update of project planning documents, essential documents, and project instructions.
- Oversee maintenance of study-specific and corporate tracking systems.
- Might be involved in regional project oversight for APAC.
Qualifications
- MPharm, RN or university/college degree in Life Sciences or an equivalent combination of education, training and experience
- Minimum 8 years’ site monitoring experience in China
- At least 2 years’ experience as Lead Monitor
- Experience supervising clinical project activities and leading clinical project teams
- Experience in oncology, gastroenterology, infectious diseases, autoimmune diseases, or any rare disease indication is preferable
- Communication, presentation, and customer-service skills
- Team building, leadership and organizational skills
- Full working proficiency in English and Chinese
- Proficiency in MS Office applications, including MS Project
工作地点
上海黄浦区腾飞元创大厦
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