Clinical Trials Administrator (CTA) 
You are a life sciences graduate, MTA, PTA or doctor's assistant. As CTA you will be responsible for the project related preparation, collection and tracking of all study data and documentation and you will provide support to all functions in Clinical Operations and assist PMs and CRAs with their project related activities. This will include setting up of systems for study conduct and handling and archiving all correspondance, study data and documentation and the preparation of status reports for sponsors.

Experience in the CRO or health care industry, as a CTA or project assistant, would be an advantage but is not essential. Fluency in Polish and a good working knowledge of English, both oral and written, good proof readng skills and a good knowledge of medical terminology are essential as would computer experience (Word, Excel, PPT). You have the ability to coordinate and prioritise, you have a good eye for detail and you are a good team player.

Clinical Research dept

Warsaw, Poland