Senior Clinical Research Associate (Experienced) | Senior Clinical Research Associates (experienced) - Germany

Job Summary

This permanent Senior Clinical Research Associate role involves defining, developing, and delivering clinical programs within the PPD clinical research portfolio, focusing on end-to-end support for clinical trials. The successful candidate will perform and coordinate all aspects of clinical monitoring and site management, conducting remote or on-site visits to ensure strict adherence to the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs. Key daily activities include applying a risk-based monitoring approach, using Root Cause Analysis (RCA) to address site process failures, and ensuring data accuracy through Source Document Review (SDR), Source Document Verification (SDV), and Case Report Form (CRF) review. This position requires strong critical thinking and communication skills, a background in life sciences, and a minimum of two years of monitoring experience. It offers flexible work arrangements (fully home-based, office-based in Munich or Karlsruhe, or hybrid) and high travel requirements (up to 50-75%) across Germany, enabling the delivery of life-changing therapies on a global scale.