
Experienced pharmacovigilance professional with expertise in ICSR processing, SAE handling, MedDRA coding, narrative writing, and aggregate reporting. Proficient in utilising databases such as ARGUS and safety reporting tools to ensure regulatory compliance with ICH-GCP, EMA, FDA, and WHO-DD standards. Strong clinical knowledge in ADR reporting, medication management, patient counselling, and drug interaction analysis. Skilled in medical writing, data documentation, and MS Office Suite to curate accurate reports and operational efficiency. Adept at team collaboration, problem-solving, time management, and advocating for patient safety. Committed to advancing healthcare standards through meticulous attention to detail and adherence to global regulations.
Effects of Polypharmacy on Medication Adherence in Hypertension & Diabetes Mellitus Patients – Published research.
Right to Work: UK visa valid until 2028