During my previous internship, I was responsible for coordinating patient visits, updating medical records, and assisting with data entry for a clinical trial. I created a detailed schedule to prioritize tasks based on urgency and deadlines. This allowed me to efficiently manage my time and ensure that all tasks were completed accurately and on time. I also communicated regularly with my supervisor to address any issues promptly.

I prioritize meticulous documentation and double-checking all data entries. I follow established protocols and guidelines strictly to avoid errors. Additionally, I maintain clear and organized records, ensuring that any discrepancies are immediately addressed and resolved. Regularly reviewing data with my team also helps in identifying and correcting any inaccuracies promptly.

I have completed coursework on Good Clinical Practice (GCP) and have hands-on experience with regulatory documentation during my previous internship. I understand the importance of adhering to ethical standards and legal requirements, such as informed consent and patient confidentiality. I am also familiar with the submission processes for Institutional Review Board (IRB) approvals and the maintenance of regulatory binders.

I believe in prioritizing patient welfare and ensuring that all research activities are conducted ethically. If faced with an ethical dilemma, I would consult with my supervisor or the ethics committee to discuss the situation and seek guidance. I would also ensure that any decisions made are in the best interest of the participants and align with the principles of GCP.

I have experience using statistical software such as SPSS and R for data analysis during my coursework and previous internship. I am proficient in performing descriptive and inferential statistics, creating data visualizations, and interpreting results. I also understand the importance of validating data and ensuring that statistical analyses are conducted according to the study protocol.