Senior Clinical Research Associate

This global clinical research organisation (CRO) has spent over four decades dedicated to driving progress in oncology. With a portfolio that spans early and late-phase cancer trials across Europe, the US and Asia, they\’ve supported over 250 studies aimed at transforming cancer into a livable disease. At the heart of their mission is a commitment to giving new cancer therapies the best chance to benefit patients – blending scientific expertise with a deep understanding of trial complexities from lab to clinic. As they continue to expand their European operations, they\’re looking for a freelance Senior Clinical Research Associate (SCRA) fluent in German and English, to play a critical role in the oversight of oncology trials in Germany. Your role as Senior Clinical Research Associate Oversee the day-to-day management of clinical sites, maintaining strong, supportive relationships with site staff and ensuring studies stay on track. Conduct pre-study visits, site initiations, routine monitoring (remote and on-site), and close-out visits in line with protocols and regulatory standards. Maintain and quality check essential regulatory documents throughout the lifecycle of studies, ensuring accurate, audit-ready records. Support preparation of study-specific tools and documents such as reports, newsletters and study manuals. Collaborate closely with project teams to ensure regulatory readiness, including aspects like contract and budget negotiations. Track study progress via clinical systems (CTMS, eTMF) to guarantee up-to-date, complete and compliant documentation. Proactively identify, troubleshoot and escalate site or data quality issues, safeguarding subject protection and data integrity. Contribute to regular project updates and reports, often juggling multiple studies at once. Experience and qualifications for the Senior Clinical Research Associate role Bachelor\’s degree (or equivalent) in a biological or human sciences field; nursing qualifications also considered. Minimum 5 years\‘ experience as a Clinical Research Associate, with a strong background in managing clinical trial sites. Solid experience in monitoring oncology trials, ideally early phase studies. In-depth knowledge of ICH-GCP and regulatory requirements, with a proven track record of ensuring compliance. Highly organised, able to multitask effectively and work autonomously within a team structure. Skilled communicator, comfortable building rapport with investigators, study teams and sponsors. Proficient in Microsoft Outlook, Word and Excel. Fluent in German and English (written and spoken). Perks and benefits Flexible freelance contract (approx. 0.4-0.5 FTE over 3 months), ideal for professionals seeking work-life balance alongside impactful projects. Chance to work on studies at the forefront of oncology innovation, contributing directly to new treatments. Collaborative, supportive teams who value expertise and autonomy. Exposure to global trial environments and sophisticated study frameworks. Ready to explore this Senior Clinical Research Associate opportunity? Apply now for immediate consideration, or reach out directly to discuss similar freelance CRA roles within oncology across Europe.