Clinical Research Associate II: On-Site Monitoring
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PSI CRO in Spain is seeking a Clinical Research Associate II to lead on-site monitoring across Phase II/III studies, ensuring data quality and regulatory compliance. You will build strong relationships with sites and investigators, manage communications with cross-functional teams, and support feasibility studies and regulatory submissions.
The role requires fluent English and Spanish, a Life Sciences degree with a Master’s in Clinical Trials, and at least 1 year of independent on-site
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