Pharmacovigilance Specialists oversee safety monitoring strategies for pharmaceuticals, biologics, and advanced therapies. They analyse aggregated safety datasets, identify emerging risk signals, prepare regulatory submissions, and collaborate with medical directors to evaluate therapeutic risk profiles. They ensure compliance with global safety frameworks and contribute to safety governance meetings, risk-minimisation plans, and clinical safety reviews. The role demands strong scientific reasoning, medical interpretation skills, and precision in documentation. Growing global regulatory scrutiny, expansion of biologics and gene therapies, and digital safety analytics are significantly expanding demand for skilled PV specialists.