Site Specialist II
Hybrid · Taipei, Taiwan, Taiwan
Job Summary
Site Specialist II at ICON Taipei Hybrid location; independently manage a range of site support activities, coordinate site-level document collection, review, and maintenance for assigned sites or studies; act as an operational liaison for site staff on documentation, systems, and process-related questions; maintain up-to-date site status, metrics, and key milestones in clinical trial management tools; support planning and logistics for site meetings, investigator meetings, and monitoring visits; identify opportunities to streamline site workflows and contribute to process improvement initiatives; provide guidance to Site Specialist I or junior colleagues, sharing best practices and supporting their development.
Required Qualifications
- Bachelor’s degree in life sciences, healthcare, business, or a related field, or equivalent clinical research experience
- Relevant experience in site support, clinical administration, or similar roles within CRO, pharma, or healthcare
- Good understanding of clinical trial processes, GCP, and site documentation requirements
- Strong organisational and problem-solving skills, with the ability to manage multiple sites and priorities
- Excellent communication and interpersonal skills, with a proactive, service-focused mindset
- Comfort working independently while collaborating effectively with cross-functional teams
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based
Additional Requirements
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
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