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.