
Biomedical Sciences graduate with experience in data collection, analysis, and documentation across research and academic settings. Currently completing a clinical research course to strengthen knowledge of Good Clinical Practice (GCP), clinical trial management, and regulatory requirements. Analytical, detail-oriented, and highly organised, with experience supporting research projects, surveys, and data-driven initiatives. Interested in applying scientific and research skills within an Entry Level role as a Regulatory Affairs Associate, Clinical Trial Assistant, Study Coordinator, or Clinical Data Administrator.
NIHR Introduction to Clinical Research (4-Module Course)- Ongoing