For our client, a very fast growing CRO with an office based in South Poland we are looking for a Clinical Research Associate to work on permanent basis.

Your main responsibilities on this position will include monitoring visits in line with documents management, study set-up and site closure, site adherence to GCP, protocols and timeliness, maintenance of the TCF and assistance in gathering documentation.

In order to apply for this position you will need to hold a life science degree or be a nursing graduate. At least one year experience on a similar role, especially experience in site assessment, initiation and monitoring across a number of protocols at GP and hospital sites is also required. Candidates will ideally have at least 2 years monitoring experience and exposure to oncology trials.


In return successful candidates will be offered a permanent role with a great salary package, company car, laptop and a mobile phone. Our client also offers an opportunity to progress within the company and a training scheme. In addition the company provides a great working environment an opportunity to work with young and dynamic teams. For further details please forward your CV to or call + 44 (0) 207 255 6600