Clinical Trials and Data Management

Service Description

Clinical Trial and Data Management: Principles, Processes, and Professional Practice This comprehensive training course is designed to equip participants with a solid foundation in the principles, processes, and best practices of clinical trial operations and clinical data management. Whether you're new to clinical research or seeking to strengthen your professional edge, this course delivers industry-relevant knowledge in a clear, structured format. Learners will explore the complete clinical trial lifecycle, from historical foundations and global regulatory frameworks (including FDA, EMA, and NAFDAC) to the application of ICH E6(R2) Good Clinical Practice guidelines. You’ll gain critical insights into study phases, stakeholder responsibilities, electronic data capture (EDC), data cleaning, database lock procedures, and outsourced study oversight. Through simplified diagrams, real-world case studies, and an end-of-course quiz, learners will build practical, job-ready skills applicable to roles in CROs, pharma companies, site management, and clinical operation,