Clinical Research Associate II

Performs and coordinates all aspects of the clinical site monitoring services, assessing for protocol and regulatory compliance. Responsibilities include driving investigative site and patient recruitment, conducting source data verification, assessing drug accountability, data collection, (regulatory) document collection, performing qualification, initiation, monitoring and close out visits at 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. Investigational Site Monitoring (55-60%) Conducts and documents site initiation, routine monitoring and close out visits, reviewing files, forms, and filings to ensure alignment with SOPs, study guidelines and GCP best practices.