CRA Required in Germany. Would You Like to Work Alongside a Full Service CRO? CRA Exp Required

As a Clinical Research Associate the successful candidate will be responsible for site qualification, initiation, interim monitoring, site management and study close out visits for studies in accordance with Good Clinical Practises (GCP's), local and international regulations and Standard Operating Procedures (SOP's) In addition, you will ensure the quality of data submitted from study sites and assure a timely submission of data. Candidates must be qualified to degree level in a relevant discipline, combined with proven previous experience working as a CRA. Extensive knowledge of three to five therapeutic areas including Alzheimer's is essential.