Who we are
We’re innovation, curiosity and diversity – multiplied by 80,000 professionals in 150 countries. As a global leader in research-focused healthcare, we’re constantly learning and growing – and seeking people who share these goals.
Garnering an expert understanding of the programs, products and strategic context that sit within your remit, in this role you will influence safety science through the development of product safety strategies in collaboration with highly talented project teams. Undertaking the review of clinical protocols, study reports and documentation you’ll be ensuring that safety science plans are closely aligned with business activities, risk management and outcomes, influencing the clinical development strategy by providing drug safety input and decision making in relation to specific products.
You’ll contribute to regulatory submissions through the rigorous review and preparation of safety data, requiring a detailed and structured approach to working with information. With an ever-changing landscape, it is also crucial that internal and external drug safety partners are involved in the process of developing drug safety plans that result in excellent outcomes for patients and you’ll be presenting and reporting on key safety issues to expert committees.