Benefit/Risk Associate Director
Anne is joint head of our Benefit/Risk team, based in Dublin. She has 15+ years experience working in pharmacovigilance in both the Contract Research Organisation setting (IQVIA, formerly Quintiles) and in a global pharmaceutical company (Aspen Pharma). During her career, Anne has worked across a wide range of pharmacovigilance tasks including case processing, literature review and analysis, aggregate report drafting and schedule management, QC, signal detection, responding to regulatory authority queries, mentoring and training, regulatory intelligence, business development and client management. In her most recent position, Anne was responsible for managing the global aggregate reporting requirements for a large portfolio of 40+ medicinal products covering a wide range of therapeutic areas. Key skills include strong scientific writing, analysis and evaluation, faultless adherence to tight regulatory timelines and proficiency in managing several ongoing projects simultaneously. Anne is a graduate of University College Dublin having been awarded a PhD in Pharmacology. Prior to her pharmacovigilance positions she worked in clinical trial data management.