Lisa Botes Email & Phone Number

On a day to day basis I am responsable for the following:·       Developing the clinical trial protocol in collaboration with the study team·       Defining study objectives, study design, inclusion and exclusion criteria, study endpoints and data collection methods·       Developing and implementing the trial plan, including creating a timeline for the study, identifying and securing the necessary resources, and managing the trial budget·       Selecting and managing clinical trial sites·       Ensuring regulatory compliance, such as FDA regulations and GCP guidelines·       Managing the study team, including assigning tasks, monitoring performance, and ensuring that the team is working effectively and efficiently·       Ensuring that the data collected during the clinical trial is accurate, complete, and of high quality·       Communicating with study sponsors, investigators, regulatory agencies, and other stakeholders to ensure that the trial is progressing as planned and to address any issues that arise during the trial·       Ensuring the safety and wellbeing of trial participants, including monitoring adverse events and ensuring that the study protocol is being followed

Listed skills include Clinical Trials, Gcp, Diabetes, Ich Gcp, and 35 others.