Senior Study Coordinator

1 semana atrás


Lisboa, Lisboa, Portugal ICON Tempo inteiro

We are seeking a Senior Study Coordinator to join our team at ICON. In this role, you will be responsible for coordinating activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation.

This includes submitting protocol, consent documents for ethics/IRB approval and assisting in preparing regulatory submissions as requested. Additionally, you will participate in preparing and reviewing study documentation and feasibility studies for new proposals as required.

You will work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV. This role is sponsor dedicated, meaning you will be working with one sponsor at a time, providing them with excellent support and service throughout the entire clinical trial process.

Key qualifications for this role include 18 months+ of independent monitoring experience in phase I-III trials as a CRA, working for a CRO or pharma company. You will possess excellent written and verbal communication skills in English and Portuguese.



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