Senior Administrative Intern For Clinical Research
- Support the Clinical Research Department with clinical trial management and completion of clinical research trials. - Track regulatory documents and correspondence, maintain study files, collect and enter study data and maintain databases, and assist in the general implementation of clinical studies. - Assist with follow up and closing of clinical studies.- Participate in monitoring visits and assist with data query resolution. - Comply with established policies, health and safety regulations and requirements, procedures, and department objectives.Protecting Human Research Participants (PHRP) Training completed on 11/05/2020.