Experienced Junior Data Analyst with a strong background in pharmacovigilance and drug safety, offering 3 years of expertise in data entry, regulatory compliance, and case processing using ARIS G and Oracle Argus databases. Proficient in medical coding (MedDRA), project management, and quality assurance. Skilled in collaborating across functions, effective communication, and problem-solving. Proven track record in generating safety reports and ensuring regulatory compliance with FDA, EMA, and MHRA standards. Recognized for contributions to high-profile projects in the pharmaceutical industry.
Database Management:
Medical Coding:
Communication:
Project Management:
PCT
General course in IPR