Clinical Trial Monitoring Essentials is an entry-level course designed for professionals starting their career as Clinical Research Associates (CRAs) or moving into clinical research from related fields. It gives a clear, practical foundation in how clinical trials are run and monitored globally: from the basics of clinical research and the roles of everyone involved in a trial, to the ethical and regulatory framework that governs it and the principles behind sound trial design. Taught through short, on-demand video lessons, the course helps learners understand the “why” behind monitoring activities and builds the core knowledge expected of a CRA working on international studies. Skills you’ll gain: - Clinical research fundamentals - Clinical trial monitoring - Understanding of clinical trial stakeholders (sponsors, CROs, sites, investigators) - Good Clinical Practice (ICH-GCP) - Regulatory affairs basics (FDA, EMA, competent authorities) - Ethics committees and informed consent principles - Regulatory submission documentation - Clinical trial design and phases