Clinical Research Associate II - Taipei

About the role

PSI CRO, a global clinical research company founded in 1995, is looking for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in Taiwan. The role is office-based in Taipei and focuses on timelines, targets and standards across a variety of therapeutic indications, while building relationships with clinical sites and investigators and protecting subjects' rights, safety and well-being.

Key responsibilities

• Conduct and report all types of onsite monitoring visits
• Take part in study startup
• Review CRFs, verify source documents and resolve queries
• Facilitate site budgets and contract negotiations
• Monitor trial progress at country level
• Manage site communication and act as a point of contact for in-house support services and vendors
• Communicate with internal project teams on study progress and participate in feasibility research
• Support the regulatory team in preparing documents for study submissions

Required profile

• College or university degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training and experience
• At least 2-3 years of independent on-site monitoring experience in Taiwan
• Experience in Phase II and/or III monitoring visits
• Experience in Multiple Sclerosis, Inflammatory Bowel Disease, Oncology or Infectious Diseases (preferred)
• Full working proficiency in English and Chinese
• Ability to plan, multitask, work in a dynamic team, communicate and collaborate, solve problems and travel

What we offer

• Training and mentorship programs
• Competitive salary and comprehensive benefits package
• Structured career development pathways