As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical clients focused on oncology studies. This exclusive partnership offers a culture of innovation, flexibility, and collaboration to bring life-improving treatments to market.

• Full ownership of investigator sites from study initiation to close-out
• Conducting feasibility, site selection, interim, and close-out visits
• Building strong relationships with investigator site staff to meet key clinical metrics
• Attending investigator meetings, ensuring proper shipment, storage, and accountability of clinical supplies
• Monitoring data integrity and compliance with clinical trial guidelines

• Stable experience as a CRA within a pharmaceutical company or CRO
• Strong expertise in Oncology (other Phase II-III commercial trial experience is also valued)
• Experience in RBM/RBQM (Risk-Based Monitoring & Quality Management)
• Excellent organizational skills and ability to adapt to a dynamic environment
• Strong IT skills and ability to multitask under pressure
• Fluency in French and professional proficiency in English
• Minimum 24 months of independent external monitoring of commercial oncology studies
• Work format: Hybrid model with 1-3 days/week at the client’s office (office-based, not on-site monitoring days)

Why Join ICON?

At ICON, we believe in empowering our Clinical Operations team. You’ll receive the support and development opportunities to grow both personally and professionally while working in an environment where your contributions truly matter. Our team thrives on collaboration, problem-solving, and strong site relationships, playing a fundamental role in advancing drug development worldwide.

Ready to take the next step? Apply now and be part of a team that’s making a real difference!

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