Key Responsibilities:

• Take full ownership of investigator sites for assigned studies, managing the site from start to close-out.
• Plan and conduct site visits (feasibility, site selection, interim, and close-out) in line with the clinical monitoring plan.
• Build and maintain effective relationships with investigator site staff to ensure key clinical metrics are met.
• Prepare for and attend investigator meetings, coordinate the timely shipment and proper storage of clinical supplies, and follow-up on drug safety issues.
• Ensure the integrity of clinical data, maintaining site tracking records and adhering to relevant guidelines.

What You Need:

• Experience as a CRA, with previous work in Oncology trials within the pharmaceutical industry or a CRO.
• Excellent organizational skills with the ability to manage multiple priorities.
• Ability to thrive in a dynamic environment, adjusting to changing business needs.
• Strong IT skills and the ability to multitask and work under pressure.
• Strong communication skills with a proactive approach to problem-solving.
• Fluency in French and professional proficiency in English.

Why Join ICON?

Our Clinical Operations team is second to none. At ICON, you will receive the support you need to grow both personally and professionally in a dynamic environment where your contributions truly matter. Our team works together to solve challenges, build strong site relationships, and achieve our shared goals. As a CRA, you will play a key role in our clients' drug development processes as part of a global study team.

Ready to make a difference? Apply today and take the next step in your career with ICON!

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