The Drug Safety Scientist provides expert analysis and interpretation of safety data from clinical trials and post-marketing surveillance. This role involves evaluating the safety profile of drug products, conducting risk assessments, and developing risk management strategies. The scientist is responsible for preparing detailed safety reports, including individual case safety reports (ICSRs) and periodic safety update reports (PSURs). They also contribute to the development of safety strategies and protocols, and collaborate with clinical and regulatory teams to ensure compliance with global regulations. The role requires advanced knowledge of pharmacovigilance and scientific principles, as well as experience in risk management and safety data analysis. Strong analytical skills, attention to detail, and the ability to interpret complex safety data are essential. Effective communication skills are required to present findings and recommendations to internal stakeholders and regulatory authorities. A degree in life sciences or a related field is necessary, with significant experience in drug safety and pharmacovigilance preferred. The role may involve occasional travel for meetings and training.