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.

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