Clinical Research Associate II
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About the role
Office-based Clinical Research Associate II role in Taipei managing clinical aspects of global projects in Taiwan. Responsibilities include onsite monitoring, study startup, CRF and source-data review, query resolution, site management, feasibility, regulatory submission support, and trial progress monitoring. Requires a college/university degree or equivalent education, training and experience, at least 2–3 years of independent onsite monitoring experience in Taiwan, Phase II/III monitoring experience, and full working proficiency in English and Chinese.
Key requirements
- • College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
- • At least 2 years of relevant experience
- • Required skills: Independent onsite monitoring, Conducting and reporting onsite monitoring visits, Study startup, CRF review, Source document verification, Query resolution, Site communication and management, Clinical trial progress monitoring, Feasibility research, Regulatory submission support, Planning and multitasking, Communication, Collaboration, Problem-solving, Ability to travel
- • Required languages: English, Chinese
Opportunity details
- • Workplace: On Site
- • Posted: Sep 23, 2026
- • Original advert language: English
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