Clinical Research Associate II (CRA II)| Germany| Hybrid

As a Clinical Research Associate (CRA II), you will play a key role in ensuring the successful delivery of clinical trials while maintaining the highest standards of GCP, ICH-GCP compliance, and regulatory requirements. You will work closely with investigative sites, study teams and external partners to ensure studies are conducted efficiently, ethically and in accordance with protocol requirements. - Conduct and manage site selection, site initiation, monitoring and close-out visits. - Ensure clinical trials are conducted in compliance with study protocols, Good Clinical Practice (GCP) guidelines, applicable regulations and standard operating procedures. - Monitor study progress, including regulatory approvals, patient recruitment, CRF completion and query management. - Review CRFs in line with the monitoring plan and study requirements. - Support communication and coordination between investigative sites and external vendors, including central laboratories. - Ensure appropriate reporting and follow-up of adverse events. - Identify, document and support the management of protocol deviations and corrective action plans. - Contribute to the preparation, review and maintenance of clinical trial documentation and study files. - Support site payment management activities. - Collaborate effectively with multidisciplinary teams to ensure successful study delivery. - Degree in a Life Sciences or Health Sciences discipline, such as Pharmacy, Biochemistry, Biology or a related field. - Master's Degree in Clinical Research or equivalent professional experience. - Previous experience working as a Clinical Research Associate (CRA) within Clinical Trials. - Strong knowledge of GCP, ICH-GCP, and current clinical trial regulations. - Fluent German and English communication skills, both written and spoken. - Willingness and availability to travel as required. - Strong organisational, planning and communication skills. - Ability to work independently while contributing effectively within a team environment.Preferred Qualifications - Previous experience in Onco-Haematology / Oncology Clinical Trials. - Additional language skills beyond English. - Permanent full-time employment contract. - Hybrid working model combining remote work and office-based collaboration. - Opportunity to join a well-established and growing organisation within the clinical research sector. - Continuous professional training and development. - Supportive leadership and a collaborative team environment. - Clear opportunities for professional growth and career progression. - Competitive salary aligned with experience, skills and qualifications. - Immediate start available. Germany Hybrid Working (combination of remote and office-based work) If you are an experienced CRA, passionate about Clinical Monitoring, Clinical Trials, and delivering high-quality research in compliance with GCP/ICH-GCP standards, we would love to hear from you. Apply today and become part of a team committed to driving meaningful progress in healthcare and clinical research.