Luminary Group is excited to announce an opportunity for a skilled Pharmacovigilance Specialist to join a top pharmaceutical company. This is a fantastic chance to contribute to patient safety by managing and reporting safety data and ensuring compliance with regulatory requirements. Responsibilities: Monitor and analyze adverse events and safety data for various drug products. Conduct thorough case reviews, documentation, and safety assessments. Prepare and submit safety reports to health authorities in compliance with relevant regulations. Participate in safety signal management and contribute to risk management plans. Work collaboratively with internal teams to facilitate timely and accurate reporting of safety information. Stay informed on current Pharmacovigilance regulations and industry standards. Assist in the development and refinement of Pharmacovigilance processes. Engage in training and mentoring roles for junior staff members. Requirements Bachelor's or higher degree in Pharmacy, Life Sciences, or a relevant field. At least 3 years of experience in Pharmacovigilance or related areas within the pharmaceutical industry. In-depth understanding of Pharmacovigilance regulations and guidelines. Experience with case processing, including data entry, coding, and writing comprehensive narratives. Proficient in using industry-standard Pharmacovigilance databases and tools. Meticulous attention to detail with a focus on data integrity. Strong analytical skills to evaluate safety data effectively. Excellent written and verbal communication skills. Ability to thrive in a fast-paced environment and manage multiple priorities. Willingness to work as part of a dynamic team while also demonstrating independence.