You will be expected to advise colleagues and clients on data interpretation and therefore should also have acquired a good understanding of the role of in vitro ADME in drug...
Manage the later-stage, commercial-enabling technical operations to meet, exceed and support business objectives for clinical cell therapies; Successfully execute the strategy and...
The Study Director is primarily responsible for the overall conduct of studies and ensuring compliance with appropriate regulations, such as ICH Q5A, and adhering to Good...
Designs and executes evidence generation activities (non-interventional, pragmatic, low-interventional and interventional Phase IIIb/IV studies) that will fill priority evidence...
We are recruiting for an Associate Director, Regulatory Affairs UK&IE to have the ownership for all new UK (UK/GB/NI) and IE Marketing Authorisation submissions for New...