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Precision Medicine Group
Clinical Research Associate/ Clinical Research Associate II
Remote · France · Mid level
About the role
Monitor and manage clinical studies at investigative sites ensuring compliance with protocols and regulations. Coordinate study setup and monitoring activities including regulatory submissions and site visits.
What you’ll do
• Monitor clinical studies at investigative sites. • Ensure studies follow protocol, SOPs, ICH-GCP. • Coordinate study setup and monitoring activities. • Identify investigators and prepare regulatory submissions. • Conduct pre-study and initiation visits.
What you’ll bring
• Life science degree or equivalent experience. • 1+ year CRA experience in CRO or pharma/biotech. • Experience managing oncology studies. • Availability for domestic travel up to 50-60%. • Excellent communication and organizational skills.
Life at Precision Medicine Group
High CRA retention rates and strong work/life balance with reasonable travel. Supportive management and impactful roles in a smaller CRO.
About Precision Medicine Group
Precision Medicine Group integrates clinical trial execution with scientific knowledge and data sciences, focusing on Oncology and Rare Disease.