Pharmacist (M.Sc.) with GCP (ICH E6 R2) certification and practical experience in both hospital and community pharmacy. Skilled in reviewing clinical and safety documentation, familiar with SAE reporting requirements, CRF/eCRF management, and working according to SOP, GMP, and GDP standards. Knowledgeable in pharmacovigilance principles, clinical data flow, and study documentation management. Organized, detail-oriented, and eager to contribute to clinical trials, pharmacovigilance, and regulatory affairs within the pharmaceutical industry.
GCP Certificate – Medical Research Agency
• Excellent attention-to-detail and ability to review complex safety data
• Motivation to develop in Clinical Trial Safety / Pharmacovigilance / Regulatory Affairs
Active lifestyle (fitness, pilates, dance), continuous language learning and cultural travel.