Established in 2014, Excelya is a contract research organisation (CRO) .
We offer a personal and authentic experience within an ambitious young healthcare company on its way to becoming the leader in clinical research in Europe with our 800 Excelyates. Our unique one-stop-shop service model – leveraging a comprehensive and functional service provider and consultancy – allows our Excelyates to evolve across a wide range of projects. Working with leading experts, Excelya advances scientific, managerial and human knowledge to improve the patient journey.
For our team members, excelling with care means enjoying a challenging professional environment that encourages personal, intellectual and operational participation so that together we can be the best in our field. We are committed to empowering each Excelyate to express their natural talents, develop their full potential and invest in our unique project.
You will be responsible for the successful conduct of clinical trials in oncology on interventional and non-interventional studies.
Your mission will therefore be as follows:
– Have carried out monitoring visits
– Knowledge of the stages of monitoring a clinical trial (selection, initiation, inclusion, follow up, closure)
– Minimum 1 year experience on clinical studies
– Experience in oncology (a plus)
– Good level of English