Clinical Research Associate II
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About the role
Hybrid, 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 review, query resolution, site management, trial progress monitoring, feasibility work, and regulatory submission support. Requires a college/university degree or equivalent education, training and experience, 2–3 years of independent onsite monitoring experience in Taiwan, Phase II/III monitoring experience, English and Chinese proficiency, and travel ability.
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 on-site clinical trial monitoring, Conducting and reporting onsite monitoring visits, Study startup, CRF review, Source document verification, Query resolution, Site communication and management, 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: Hybrid
- • Posted: Oct 19, 2026
- • Original advert language: English
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