div h3 Build our future together: /h3 p As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs staff, support cross functional and external partners, and serve as a key liaison in regulatory authority interactions. /p h3 Where and when: /h3 p This is a Uxbridge based position and will require you to be on site 3 days per week and 2 days from home. A fully remote role is not possible for this position. If eligible, we can offer relocation benefits. /p h3 Discover your role: /h3 ul li Lead product development activities from a CMC regulatory standpoint with input from senior management. /li li Represent CMC RA at program meetings and independently provide regulatory interpretation, position, and coverage of clinical development, initial market applications, and approval/post approval acti...