In-House Clinical Research Associate (Poland)

This position will support and observe clinical site monitoring services inhouse and provide monitoring and site management activities for full-service studies assessing for protocol, SOP and regulatory compliance. Responsibilities include site management activities to help drive investigative sites and patient recruitment, compliance and oversight.  Conduct remote data review, support data query and closure activities, support Risk Based Monitoring (RBM) activities, assess data collection and (regulatory) document collection, perform remote activities for investigational sites in accordance with corporate, sponsor and regulatory (ICH GCP and other) standards and guidelines. Represents the corporation by maintaining collaborative relationships with stakeholders.