Clinical Research Associate

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

Bachelors 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 environment focused on improving access to life-changing therapies worldwide.