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Precision Medicine Group
Clinical Research Associate II
Remote · Netherlands · Mid level
About the role
Monitor and own progress of clinical studies at investigative sites ensuring compliance with protocols and regulations. Coordinate activities for study setup and monitoring including regulatory submissions and site visits.
What you’ll do
• Monitor clinical studies per protocol and regulations. • Coordinate study setup activities. • Conduct pre-study and initiation visits. • Identify investigators and assist regulatory submissions. • Ensure quality and outcomes of work.
What you’ll bring
• Life science degree or equivalent experience. • 2+ years CRA experience in CRO or pharma/biotech. • Availability for domestic travel up to 60%. • Fluency in English and Dutch. • Excellent communication and organizational skills.
Life at Precision Medicine Group
High CRA retention rates with reasonable travel and good work/life balance. Smaller CRO with impactful roles and supportive management.
About Precision Medicine Group
Precision Medicine Group integrates clinical trial execution with scientific knowledge and data sciences, focusing on Oncology and Rare Disease.