Clinical Trial Implementation: Site Initiation, Subject Recruitment, Monitoring and Safety Reporting

The third in a series of four courses, this course is designed to deepen your knowledge of the processes and procedures to implement clinical trials. The role of clinical trial monitors is highlighted in a detailed review of the various aspects of study monitoring, such as data review, safety reporting and drug accountability. You also review global drug development and issues such as subject recruitment and retention (which are crucial to meeting study timelines and regulatory requirements), site initiation processes, and setting up trial master files and investigator files.