Clinical Research Associate II

We are partnering with a leading clinical research organisation to support their search for an experienced Clinical Research Associate (CRA) based in Germany. Our client is a mid‑sized CRO that’s outperforming the market this year through repeat business, multi‑sponsor studies, and a reputation for quality delivery. Working in onsite monitoring, they are offering real progression opportunity in a business that gives back to its team. It’s a great balance - the scale and stability of a high‑performing CRO, but the autonomy and close‑knit feel of a mid‑sized business. Key Responsibilities: Manage assigned clinical trial sites and act as the primary site contact. Conduct site monitoring visits (PSV, SIV, routine monitoring, and close‑out visits). Ensure studies are conducted in compliance with protocols, ICH‑GCP, regulatory requirements, and SOPs. Support site start‑up activities, including feasibility and site selection. Review and maintain essential regulatory documentation. Monitor patient enrolment, site performance, and investigational product accountability. Provide regular site updates to the project team and contribute to study success. Requirements: Previous clinical research experience, including independent monitoring experience in Germany. Strong knowledge of ICH‑GCP and regulatory requirements. Fluent in German and English (written and spoken). Excellent organisational and communication skills. What's on Offer: Opportunity to join a global and collaborative clinical research environment. Strong focus on professional development and career progression. Flexible working arrangements and a supportive team culture. The chance to contribute to innovative clinical research that improves patient outcomes. Incentive bonus schemes that pass the business success directly back to the team. #J-18808-Ljbffr