Monitor and own progress of clinical studies at investigative sites.
Coordinate site setup, monitoring visits and regulatory tasks.
Ensure studies are conducted, recorded, and reported per protocol, SOPs, and ICH-GCP.
Remote-based role in France with travel to sites; based in Paris/Paris area.

🎯 Requirements

Life science degree and/or equivalent experience
1 year+ CRA experience in CRO or pharma or equivalent
Experience managing oncology studies
Availability for domestic travel up to ~50-60%
Fluency in English and local language where based

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