Graduate Intern - Clinical Operations Specialist

Clinical Trials-focused Graduate Intern role supporting planning, coordination, and delivery of clinical studies at country level in line with ICH GCP and local regulations. Responsibilities include defining regulatory submission strategies, preparing and tracking submission documents, coordinating with authorities and ethics committees, managing clinical trial supplies and logistics (including import/export and cold chain if applicable), overseeing site payments and vendor management, ensuring timely study budgets and forecasts, supporting audits and SOP compliance, and leveraging digital/AI tools to improve efficiency and decision-making. Requires cross-functional collaboration and strong communication in a life sciences background. On-site in Johannesburg, South Africa with some hybrid flexibility.