The Associate Director of Regulatory Affairs Strategy will work on assigned programs with the respective Global Regulatory Portfolio Lead, Global Regulatory Lead and cross-functional team to lead the regulatory strategy and facilitate submission of data packages to the EMA. The role
The Associate Director Study Management (AD Clinical Operations) is responsible for leading a team of Global Trial Leaders and Trial Managers within the Study Management Organization. The position is responsible for staff development and study oversight, and
About This Role: As a Senior Pharmacovigilance (PV) Scientist, you will play a pivotal role as a product lead within the Safety team, overseeing and spearheading critical PV activities. Your responsibilities encompass managing the safety signal
Alnylam Pharmaceuticals in Maidenhead seeks an Associate Director, Clinical Pharmacology to provide strategic clinical leadership for RNAi therapeutic programs. You will oversee study design, planning, and execution, align cross-functional teams, and ensure regulatory compliance across development stages. This