CTI Clinical Trial and Consulting Services seeks a Clinical Research Associate to oversee monitoring activities at assigned study sites in Germany. You will ensure quality deliverables and regulatory compliance while coordinating with cross‑functional teams.
The role involves site visits (PSV, SIV, IMV, COV), regulatory documentation, and ongoing collaboration with project teams. 3‑5 years CRA experience and fluent English are required.
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Coordonnées :
Équipe de recrutement de CTI Clinical Trial and Consulting Services
