Syneos Health in Barcelona is seeking a CRA I/II for sponsor-dedicated trials.
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You will conduct site qualification, initiation, monitoring, and close-out visits onsite or remotely, ensuring GCP compliance and data integrity across trials.
The role requires a Bachelor’s degree or RN and independent CRA experience, with strong communication and willingness to travel up to 75%.
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Oncology experience is preferred as you support general studies with rigorous QA and regulatory adherence.
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📌 CRA I/II: Site Monitoring & Trial Coordination Barcelona (España)
🏢 Syneos Health
📍 España
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