Pharmacovigilance Scientist

We have a current opportunity for a Pharmacovigilance Scientist for one of our Life Science client - a leading organization in the pharmaceutical industry, dedicated to ensuring patient safety and regulatory compliance. To strengthen their Global Pharmacovigilance team, we are looking for an experienced Pharmacovigilance Scientist.Key ResponsibilitiesICSR Processing: Assess validity, code information, perform follow-up, and ensure timely reporting to health authorities.Database Management: Maintain and update the safety database to ensure accuracy and compliance.Safety Reporting: Contribute to periodic safety reports (PBRERs, DSURs, etc.).Quality & Compliance: Adhere to SOPs, KPIs, and Good Pharmacovigilance Practices (GVP) regulations.Signal Management: Support identification and evaluation of potential safety signals.Stakeholder Collaboration: Work closely with internal teams and external partners, including CROs.Your ProfileBachelor's degree in a medical, pharmaceutical, or scientific discipline.Minimum of 2-5 years' experience in a pharmacovigilance environment.Solid knowledge of GVP regulations and case processing.Strong communication skills and ability to work independently.Advanced computer and database management skills.