Site Specialist II
Hybrid · Madrid, Madrid, Spain or Barcelona, Catalonia, Spain
Job Summary
Site Specialist II at ICON in Madrid or Barcelona, Spain (office or homebased) focusing on coordinating site-level document collection, review, and maintenance with accuracy and compliance; acting as operational liaison for site staff on documentation, systems and processes; maintaining up-to-date site status, metrics, and milestones in clinical trial management tools; supporting planning and logistics for site meetings, investigator meetings, and monitoring visits; identifying opportunities to streamline site workflows and contribute to process improvements; providing guidance to Site Specialist I or junior colleagues and supporting their development.
Required Qualifications
- Bachelor’s degree in life sciences, healthcare, business, or related field, or equivalent clinical research experience
- Fluent in English and Spanish
- 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
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