Pharmacovigilance Manager

Role Description This is a part-time Pharmacovigilance Manager role based in Abu Dhabi Emirate, United Arab Emirates, with a hybrid work arrangement that allows some work from home. The Pharmacovigilance Manager will oversee the collection, evaluation, and reporting of adverse events and safety data for pharmaceutical products. Responsibilities include maintaining compliance with local and international pharmacovigilance regulations, preparing and submitting safety reports, and ensuring timely communication with regulatory authorities and internal stakeholders. The role involves developing and updating pharmacovigilance procedures, training colleagues on safety reporting requirements, and collaborating with medical, regulatory, and quality teams to mitigate risk. The manager will also support audits and inspections, maintain accurate documentation, and contribute to continuous improvement of safety systems and processes. Qualifications • Strong knowledge of Regulatory Requirements and Regulatory Affairs relevant to pharmacovigilance and drug safety. • Background in Pharmacy and Pharmaceuticals with practical understanding of medicinal products and their lifecycle. • Solid foundation in Medicine or related life sciences to interpret clinical data and safety profiles. • Experience in pharmacovigilance operations, including adverse event reporting, signal detection, and risk management. • Familiarity with international guidelines (e.g., EMA, FDA, ICH, WHO) and local UAE regulatory frameworks. • Excellent analytical, documentation, and organizational skills, with attention to detail and data integrity. • Strong written and verbal communication skills in English; Arabic proficiency is an advantage. • Ability to work independently in a hybrid setting and collaborate effectively with cross-functional teams. • Relevant university degree in Pharmacy, Medicine, or Life Sciences; advanced training or certification in pharmacovigilance is a plus. • Prior experience in a pharmacovigilance, drug safety, or regulatory role within the pharmaceutical or healthcare sector preferred.