Clinical Research Associate II
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About the role
Hybrid, office-based CRA II role in Taipei managing clinical aspects of global projects in Taiwan. Duties include onsite monitoring, study startup, CRF and source-data review, query resolution, site management, feasibility, regulatory submission support and stakeholder communication. Requires a college/university degree in Life Sciences, Pharmacy, RN or an equivalent combination of 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 availability.
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 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: Nov 10, 2026
- • Original advert language: English
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