Senior Clinical Research Associate

Pharmaceutical Research Associates, Inc; Paris; Hybride; EUR 40 000 - 80 000; Plein temps

Résumé du poste

An established industry player is seeking experienced Clinical Research Associates to join their dedicated team in Paris. This role focuses on oncology studies, offering a unique opportunity to work closely with a global pharmaceutical client. You will take full ownership of investigator sites, ensuring data integrity and compliance while fostering strong relationships with site staff. This innovative firm values collaboration and problem-solving, providing an environment where your contributions can significantly impact the advancement of life-saving treatments. If you are passionate about clinical research and looking to grow in a dynamic setting, this is the perfect opportunity for you.

Qualifications

• Stable experience as a CRA in a pharmaceutical company or CRO.
• Minimum 24 months of independent external monitoring of oncology studies.

Responsabilités

• Full ownership of investigator sites from study initiation to close-out.
• Conducting feasibility, site selection, and monitoring visits.

Connaissances

Oncology expertise

Risk-Based Monitoring (RBM)

Organizational skills

IT skills

Fluency in French

Professional proficiency in English

Description du poste

Overview

Join ICON plc as a Clinical Research Associate (CRA) in Paris/Ile-de-France!

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we drive clinical research forward by providing outsourced services to pharmaceutical, biotechnology, medical device, and public health organizations. With patients at the heart of everything we do, we accelerate the development of life-saving treatments that improve quality of life.

We are looking for experienced and motivated CRAs to join our sponsor-dedicated team!

Responsibilities

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

Qualifications

• 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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