Senior CRA
Taipei, Taiwan

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

Office-Based in Taipei, Taiwan

You will :

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Be a point of contact for in-house support services and vendors
  • Supervise study activities, project timelines and schedules on a country level
  • Participate in quality control and compliance monitoring
  • Communicate with internal project teams regarding study progress
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions
  • Qualifications

  • College / University degree in Life Sciences or an equivalent combination of education, training & experience
  • At least 4 years of independent on-site monitoring experience in Taiwan
  • Participation in clinical porjects as a Lead Moniotr
  • Prior exposure to project start-up activities, including regulatory submissions
  • Experience in Oncology, Hematology, Infectious Diseases, Gastoenterology and / or Neurology
  • Experience of working with Hong Kong and / or Chinese Investigators and sites is a plus
  • Full working proficiency in English
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel
  • 申請
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