Clinical Research Associate (m/w/d)

Start now with Randstad professional solutions! On behalf of our business partner from Berlin, we are currently looking for an experienced freelance Clinical Research Associate (CRA) to monitor and ensure the quality of clinical trials and your expertise in monitoring clinical research projects of phases I-IV. The project is initially set to 6 months with the option of extension. Parttime employment (50-80%). Apply now directly onine - our experts are looking forward to you!

Monitoring of clinical testing centres: carrying out initial, monitoring and final visits on site or remotely to ensure compliance with test protocols, good clinical practice (GCP) and regulatory requirements Source data verification (SDV): verification of compliance of data in the case report forms (CRF) with the patient data of the test centres Documentation and reporting: Precise reports on visits and communication with test centres and documentation of all relevant processes in the Trial Master File (TMF) Communication: Close cooperation with test physicians and test personnel to clarify questions, training and ensure progress in the study Deficiency detection and clarification: Identification and solution of deviations, discrepancies and errors in the test sequence and in the data

Completed studies in life sciences, medicine, pharmacy or comparable training Evidence of professional experience as a Clinical Research Associate in the pharmaceutical or biotechnology sector Comprehensive knowledge of good clinical practice (GCP), ICH policies and national laws Strong analytical skills and detailed working Embossed communication and organisational skills

Attractive possibilities to shorten your personal payment destination No more time-consuming billing required Fast, reliable fee payment Complete project contracts with electronic signature JOBV1_EN