Clinical Research Associate

**This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Research Associate based in France.** This is an exciting opportunity for a clinical research professional to contribute to innovative oncology and hematology studies with a direct impact on patient outcomes worldwide. The role combines hands-on site monitoring responsibilities with strategic collaboration across clinical operations, ensuring studies are delivered efficiently, compliantly, and with the highest quality standards. Working in a dynamic and international environment, you will support the full clinical trial lifecycle, from feasibility assessments and site initiation through study closeout. This position offers significant exposure to cutting-edge research programs, cross-functional teamwork, and opportunities to drive continuous improvement and operational excellence in clinical development. ### Accountabilities: - Conduct site feasibility assessments, identification, selection, and evaluation activities to support successful study initiation and recruitment planning. - Perform all monitoring activities, including pre-study, site initiation, routine monitoring, co-monitoring, and closeout visits in compliance with ICH-GCP guidelines and internal procedures. - Deliver protocol and study-related training to investigative sites while maintaining regular communication and providing ongoing support throughout the study lifecycle. - Track site performance metrics, including regulatory submissions, patient recruitment, CRF completion, and query resolution to ensure milestones are achieved on time. - Ensure inspection readiness by maintaining high-quality documentation standards and supporting audits, Study Oversight Visits, and regulatory inspections when required. - Identify risks, quality concerns, and operational gaps, proposing corrective and preventive actions (CAPAs) to enhance study execution and compliance. - Collaborate closely with Clinical Operations teams and site personnel to drive study progress, optimize site performance, and promote innovative solutions to operational challenges. ## Requirements - Bachelor's degree in a scientific discipline or a related field. - Minimum of 2 years of Clinical Research Associate monitoring experience within the pharmaceutical, biotechnology, or CRO industry. - Solid understanding of clinical trial processes, ICH-GCP guidelines, and applicable regulatory requirements. - Previous experience in oncology and/or hematology clinical trials is strongly preferred. - Experience supporting study start-up activities is considered an advantage. - Excellent organizational skills with the ability to manage multiple priorities and work independently in a fast-paced environment. - Strong analytical mindset with the ability to identify issues, assess risks, and implement effective solutions. - Excellent communication and interpersonal skills, with the ability to build strong relationships with investigative sites and cross-functional teams. - Fluency in both French and English, written and spoken. - Proficiency with Microsoft Office tools, including Word, Excel, PowerPoint, Outlook, and project management applications. - Willingness and ability to travel up to 60% within the assigned region. ## Benefits - Competitive salary package ranging from **€43,000 to €53,700 annually**, depending on experience and qualifications. - Fully remote position based in France, offering flexibility and autonomy. - Opportunity to work on innovative global oncology and hematology programs with meaningful patient impact. - Exposure to international clinical development projects and collaboration with multidisciplinary teams. - Continuous learning opportunities, professional development programs, and career advancement prospects. - Inclusive and collaborative work culture that values innovation, excellence, and professional growth. - Participation in a mission-driven env…