For a global, full-service Clinical Research Organisation (CRO) specialising in a wide range of therapeutic areas, we are looking for an experienced Clinical Research Associate. They are rapidly growing and active in more than 40 countries around the globe.
The Clinical Research Associate, is driven, proactive and most of all experienced in the sector. You will join a team with relatively junior CRA’s which will ask for your support and guidance to take this team to the next level. For this role you will travel up to 60% to 80% on a national level.
In this role you will be responsible for, among others, tasks related to pre-study, initiation, monitoring, and closeout visits for research sites. Additionally you will perform source document verification and case report form review, regulatory document review, conduct study drug inventory, perform adverse event and serious adverse event reporting and follow-up, and assess patient recruitment and retention.
If you are interested in this job, or in similar ones, please feel free to contact me directly.
Senior Associate Clinical Research | Medical Devices