Academic Research Coordinator

Coordinate and manage all aspects of clinical trials, including protocol development, feasibility assessments, and study design. Ensure compliance with IRB/FDA standards by overseeing subject enrollment, randomization, and reporting of adverse events. Maintain accurate study data, complete Case Report Forms, and respond to queries from sponsors and internal teams. Assess potential subjects against inclusion and exclusion criteria while supporting hospital staff in protocol adherence. Develop preliminary study budgets and assist with manuscript preparation and scientific presentations.