Study Startup Specialist I

About the role

Hybrid Study Startup Specialist I role in Taipei supporting clinical trial start-up activities in Taiwan, including site contracts and budgets, regulatory and ethics submissions, start-up timelines, site activation milestones, communications, translations, and Trial Master File maintenance. Requires at least one year of clinical development experience including start-up experience, a bachelor’s degree or above, English and Chinese proficiency, communication skills, and Microsoft Office proficiency.

Key requirements

• • Bachelor’s degree or above, preferred in pharmaceutical/healthcare related majors
• • At least 1 year of relevant experience
• • Required skills: Clinical trial start-up processes, Site budget facilitation, Contract negotiation support, Regulatory document collection, Ethics committee submission dossier preparation, Site submission dossier preparation, Study start-up tracking systems, Site-specific start-up timelines, Enrollment projections, Trial Master File maintenance, Written and verbal communication, Microsoft Office
• • Required languages: English, Chinese

Opportunity details

• • Workplace: Hybrid
• • Posted: Nov 2, 2026
• • Original advert language: English

Full vacancy

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