Study Startup Specialist I

About the role

Hybrid Study Startup Specialist I role in Taipei supporting clinical study start-up in Taiwan. Responsibilities include tracking start-up activities, facilitating site budgets and contracts, collecting regulatory documents, communicating with project teams and sites, maintaining timelines and enrollment projections, reviewing translations, and maintaining the Trial Master File. Requires at least one year of clinical development experience including start-up, a bachelor’s degree or above, English and Chinese proficiency, communication skills, and MS 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 development experience, clinical trial start-up process experience, excellent written and verbal communication, MS Office proficiency, site budget and contract negotiation support, regulatory document collection, clinical trial start-up tracking, investigational site communication, Trial Master File maintenance
• • Required languages: English, Chinese

Opportunity details

• • Workplace: Hybrid
• • Posted: Oct 19, 2026
• • Original advert language: English

Full vacancy

HealthRoleIQ regularly verifies this opportunity against the employer’s posting and highlights the details relevant to your match.