Nothando Magagula

Background

About Nothando Magagula

I worked as a Research assistant in vaccine study for adolescents and administering of informed consents, review of translated informed consents. As a Research Assistant I was involved in observational studies and other administrative duties. I have worked as a Quality Assurance officer mainly doing the quality assurance and quality control of the site, on site monitoring of all the departments, SOP review, training staff, and trend analysis. I have good administrative skills, interpersonal, verbal communication skills, attention to detail, team player, business acumen and computer skills. As a Research Operations Assistant I have taken over the duty of applying for Export permits as well as Follow up. I have also experience in submitting SAE to Ethics committees as well as to the MCC. In addition to Administrative duties as preparing for MCC or Ethics Submission I have experience in working with sites to acquiring documents. I also have experience is doing Protocol amendments and preparation for Submission. I was a Clinical Trial Specialist. Currently I am a clinical research associate GOALS: I am very interested in the Clinical Research field. I want to explore as many positions in order to learn and grow in the industry.