Clinical Research Professional with +15 years of experience: Clinical Trials Operations, Risk Management, Study Monitoring, Staff Training, Quality Assurance. Started my career as a Study Coordinator, then worked for many years as a Clinical Research Associate. Developed my skills in other positions such as Proposal Developer, Study Clinical Lead, Site Director, Risk Based Quality Manager, Clinical Operations Lead, CRA development training program manager. Most recently founded Recepta Clinical Research, a consulting business helping aspiring Investigators and Study Coordinators to navigate the ever evolving industry of Clinical Trials! With my Clinical Trials Site Operations Course I hope to help the upcoming members of the industry with valuable information about the key processes involved in running a clinical trial at site.