IdiPAZ seeks a Clinical Research Associate and Project Manager

As a clinical research associate you will be responsible for monitoring activities such as initiation visits, monitoring
visits, close-out visits, ensure the study staff conducting the protocol receive all materials and instructions to safely
enter patients into the study, review progress of projects and initiate appropriate actions to achieve target objectives,
interact with internal work groups to evaluate needs, resources and timelines, act as contact for clinical trial
suppliers and other vendors as assigned, complete process of Serious Adverse Event (SAE) reporting, process
production of reports, narratives and follow up of SAEs, independently perform CRF reviews, generate queries and
resolve issues.
You will also be in involved in the management activities of a European funded project.