Clinical Trial Administrator

仕事内容

Company Description

PSI is a leading Contract Research Organization with more than 22 years in the industry /on the market, 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

Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.

Office-based in Taipei, Taiwan

You Will

• Be the point of contact for investigational sites, vendors, and multi-functional project teams
• Be responsible for document management
• Update and maintain (automated) tracking systems and schedules
• Coordinate various activities within clinical research projects
• Organize meetings, prepare agendas and minutes

Qualifications

• Minimum 1 year experience as CTA in other CRO companyies.
• Eligible to work in Taiwan.
• College/University degree. Life Sciences degree is a plus
• Administrative work experience, preferably in an international setting
• Prior experience in Clinical Research
• Fluency in English and Mandarin
• PC skills to be able to work with MS Word, Excel and PowerPoint
• Ability to plan, multitask and work in a dynamic team environment
• Communication and collaboration skills
  

Additional Information

Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company