Pharmacovigilance Associate
CurrentAs a dedicated Pharmacovigilance Associate, I take on a critical responsibility – to ensure the smooth and prompt reporting of adverse events. With unwavering commitment to regulatory regulations and minute attention to detail, I diligently gather and forward adverse event reports, encompassing a wide range of initial, follow-up, serious, non-serious, solicited, and non-solicited cases. With a commitment to both corporate protocols and local regulations, I carefully execute each step, cognizant of the vital necessity of accuracy. Embodying my commitment to clarity and accuracy, I skillfully construct detailed and concise follow-up requests for these reports, highlighting my proficiency. Building a solid foundation of accuracy and upholding our commitment to procedural excellence, I document each ICSR-related activity in our Global PV database. In my role, I safeguard the future of our information by diligently maintaining the PV filing and archiving system. By managing these important tasks, I contribute to maintaining our rigorous standards. Together with our Sanofi CHC PV Lead, I contribute a crucial role in quarterly information compilation, adhering to essential documentation procedures. Also, I am fully invested in the maintenance and upkeep of SOPs, actively participate in aligning our Pharmacovigilance methods and encouraging a dedication to ceaseless improvement.