● To perform case intake and triage of the incoming safety information or reports from various sources either spontaneously or from a clinical trial. • Data entry of safety data onto adverse event tracking systems.• Write patient narratives & code adverse events accurately using MedDRA (for Marketed products, if applicable).• Assist in the listedness assessment against appropriate label (for Marketed products, if applicable).• Assist in generation of queries and collection of missing or discrepant information in consultation with medical staff.• Assist with processing and submission of expedited and periodic reports to worldwide regulatory agencies or other recipients (Clients, Regulatory Authorities, Ethics Committees, investigators and company project personnel etc), and prioritize the reports for processing and submission within the regulatory and/or study specific applicable timelines.

● Reviewed prescriptions and dispensed drugs accurately. ● Organized and maintained pharmacy inventory. ● Counseled patients on medication use and health management. ● Managed stock levels and ensured timely replenishment. ● Enhanced patient satisfaction through effective communication and service

During my internship in the General Medicine, General Surgery, Obstetrics and Gynaecology, and Pediatrics departments, I was responsible for:- Attended routine ward rounds and outpatient department duties.- Detecting adverse drug reactions (ADRs)- Checking for drug interactions- Promoting the rational use of antibiotics- Providing patient counsellingOver the course of the year, I completed four projects with responsibilities including:- Obtaining informed consent from subjects.- Preparing research protocols, including literature reviews and defining methodologies- Collecting and entering data into Case Report Forms (CRF).- Preparing theses and manuscripts.- Conducting knowledge assessments.- Presenting project findings.