Overview:
Join ICON plc as a Senior Clinical Research Associate in Paris & join our sponsor-dedicated team!
Responsibilities:
As a Senior 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 Senior 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
* Work format: Hybrid model with 1-3 days/week at the client's office (office-based, not on-site monitoring days)
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