Clinical Research Associate II
HybridTaipei, Taiwan, Taiwan
Taipei, Taiwan, TaiwanHybridFull TimeMid LevelBIOTECHLarge
Full TimeMid LevelLargeBIOTECH
Job Summary
Conduct onsite monitoring visits, manage study startup, and perform CRF review and source document verification. Facilitate site budgets and contract negotiations while monitoring trial progress at the country level. Build relationships with clinical sites and investigators, ensuring subject rights, safety, and data compliance. Act as a point of contact for internal teams, vendors, and regulatory document preparation. Manage feasibility research and communicate study progress across stakeholders. Requires 2-3 years of independent monitoring experience in Taiwan with proficiency in English and Chinese. Located in Taipei.
Required Qualifications
- College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
- At least 2-3 years of independent on-site monitoring experience in Taiwan
- Experience in all types of monitoring visits in Phase II and/or III
- Full working proficiency in English and Chinese
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
Desired Qualifications
- Experience in Multiple Sclerosis, Inflammatory Bowel Disease, Oncology, Infectious Diseases (preferable)
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