Supervisor, Pharmacovigilance

**Overview**:- As a Supervisor Pharmacovigilance you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. Working in this program you will feel challenged and supported to advance in your professional career while making a truly impact.**Responsibilities**:**What you will be doing**:- Supervising the day-to-day pharmacovigilance operations, ensuring timely and accurate reporting of adverse events.- Collaborating with cross-functional teams, including clinical operations and regulatory affairs, to optimize pharmacovigilance processes.- Ensuring compliance with global regulatory requirements and internal standard operating procedures for safety reporting.- Managing safety data collection, analysis, and submission to regulatory authorities.- Providing leadership and training to the pharmacovigilance team, ensuring adherence to best practices in safety monitoring.**Qualifications**:**You are**:- Bachelor’s degree in life sciences, pharmacy, or a related field.- Experience in pharmacovigilance or drug safety, with a focus on clinical trials or post-marketing surveillance.- Strong knowledge of global pharmacovigilance regulations and guidelines.- Excellent communication, leadership, and organizational skills, with the ability to manage a team effectively.- Detail-oriented with the ability to manage multiple tasks and ensure accuracy in safety reporting.**What ICON can offer you**:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.