Study Startup Specialist I
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About the role
PSI seeks a full-time Study Startup Specialist I in Taipei to support clinical trial start-up activities in Taiwan, including contracts, budgets, regulatory documentation, site activation timelines, communications, translations, and TMF maintenance. Candidates need at least one year of clinical development experience with start-up experience, a bachelor’s degree or above, English and Chinese proficiency, and MS Office skills.
Key requirements
- • Bachelor’s degree or above, preferred in pharmaceutical/healthcare related majors
- • At least 1 year of relevant experience
- • Required skills: Clinical development experience including study start-up processes, Site budget and contract negotiation support, Regulatory document collection, Clinical trial start-up tracking, Communication with project teams and investigational sites, Site-specific start-up timelines and enrollment projections, Trial Master File maintenance, Microsoft Office proficiency
- • Required languages: English, Chinese
Opportunity details
- • Workplace: On Site
- • Employment: Permanent
- • Posted: Sep 23, 2026
- • Original advert language: English
Full vacancy
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Employer’s role description
Job title: Study Startup Specialist I
Location: Taipei, Taiwan
Employment type: Full-time
Company Description
PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.