About this role
Join us <div style="font-family:'Segoe UI';font-size:14px;font-style:normal;font-weight:400;line-height:20px;">As a <strong>Clinical Research Associate (CRA II)</strong>, you will play a key role in ensuring the successful delivery of clinical trials while maintaining the highest standards of <strong>GCP</strong>, <strong>ICH-GCP compliance</strong>, 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.</div> Key Responsibilities <div style="font-family:'Segoe UI';font-size:14px;font-style:normal;font-weight:400;line-height:20px;"><ul><li>Conduct and manage <strong>site selection, site initiation, monitoring and close-out visits</strong>.</li><li>Ensure clinical trials are conducted in compliance with study protocols, <strong>Good Clinical Practice (GCP)</strong> guidelines, applicable regulations and standard operating procedures.</li><li>Monitor study progress, including regulatory approvals, patient recruitment, CRF completion and query management.</li><li>Review CRFs in line with the monitoring plan and study requirements.</li><li>Support communication and coordination between investigative sites and external vendors, including central laboratories.</li><li>Ensure appropriate reporting and follow-up of adverse events.</li><li>Identify, document and support the management of protocol deviations and corrective action plans.</li><li>Contribute to the preparation, review and maintenance of clinical trial documentation and study files.</li><li>Support site payment management activities.</li><li>Collaborate effectively with multidisciplinary teams to ensure successful study delivery.</li></ul></div> Essential Requirements <div style="font-family:'Segoe UI';font-size:14px;font-style:normal;font-weight:400;line-height:20px;"><ul><li>Degree in a Life Sciences or Health Sciences discipline, such as Pharmacy, Biochemistry, Biology or a related field.</li><li>Master's Degree in Clinical Research or equivalent professional experience.</li><li>Previous experience working as a <strong>Clinical Research Associate (CRA)</strong> within <strong>Clinical Trials</strong>.</li><li>Strong knowledge of <strong>GCP</strong>, <strong>ICH-GCP</strong>, and current clinical trial regulations.</li><li>Fluent German and English communication skills, both written and spoken.</li><li>Willingness and availability to travel as required.</li><li>Strong organisational, planning and communication skills.</li><li>Ability to work independently while contributing effectively within a team environment.</li></ul><strong>Preferred Qualifications<br></strong></div><ul><li>Previous experience in Onco-Haematology / Oncology Clinical Trials.</li><li>Additional language skills beyond English.</li></ul> What we offer <div style="font-family:'Segoe UI';font-size:14px;font-style:normal;font-weight:400;line-height:20px;"><ul><li>Permanent full-time employment contract.</li><li>Hybrid working model combining remote work and office-based collaboration.</li><li>Opportunity to join a well-established and growing organisation within the clinical research sector.</li><li>Continuous professional training and development.</li><li>Supportive leadership and a collaborative team environment.</li><li>Clear opportunities for professional growth and career progression.</li><li>Competitive salary aligned with experience, skills and qualifications.</li><li>Immediate start available.</li></ul></div> Location & Working Model <div style="font-family:'Segoe UI';font-size:14px;font-style:normal;font-weight:400;line-height:20px;"><strong>Germany</strong><br><strong>Hybrid Working</strong> (combination of remote and office-based work)</div> Ready for Your Next Career Move? <div style="font-family:'Segoe UI';font-size:14px;font-style:normal;font-weight:400;line-height:20px;">If you are an experienced <strong>CRA</strong>, passionate about <strong>Clinical Monitoring</strong>, <strong>Clinical Trials</strong>, and delivering high-quality research in compliance with <strong>GCP/ICH-GCP standards</strong>, we would love to hear from you.<br>Apply today and become part of a team committed to driving meaningful progress in healthcare and clinical research.</div>