I am a lifelong learner having completed up to a Master of Science in Medicine degree. In addition, I have also completed a Diploma in Project Management and various courses within the clinical research environment. Furthermore, during my honour’s year at Wits University, I completed a module in clinical trials which covered clinical research aspects such as, how a protocol is designed, monitoring a study, how to report adverse effects and good clinical practice, which gives me the ability to be well versed and aware of how clinical trials are carried out. I am proficient in writing detailed reports and managing laboratory projects to meet project objectives, timelines, and budget requirements. My background includes working as a Research Coordinator and Research Assistant where my primary duties included performing a wide and complex variety of assays, tests, and studies as well as provide subject-specific research expertise, writing up results and contributing to publishing of results in high quality peer-reviewed academic literature. I have gained the ability to integrate superior organization and communication skills across all levels of research, allowing me to excel in both independent and team-oriented environments. My complementary abilities in data verification, quality control, and documentation are certain to render me an immediate asset.