Regulatory Affairs Manager leads and manages a team of regulatroy affairs staff. Responsible for staffskill development, performance management and resource allocation in order to …
Core Accountabilities To obtain and maintain regulatory approval of product registration in Taiwan and work according to Good Regulatory Practice (GRP). To liaise with Emerging …
This is what you will do: Under the direction of Director, Quality Lead for Clinical Development Country Operations, the Associate Director, Quality Operations Lead (AD, QOL) is…
The Patient Safety Specialist is an appropriately qualified person for pharmacovigilance who contributes to the core components of the local pharmacovigilance system, thus ensuring…
The Patient Safety Manager is an appropriately qualified person for pharmacovigilance who is responsible for the local pharmacovigilance system, thus ensuring AZ have in place an e…
DSMM is accountable for delivering the committed part of oncology and and haematology clinical interventional studies under their supervision according to agreed resources, budget …
Field-based position responsible for developing and enhancing professional relationships with healthcare professionals. Provides scientific, technical and pharmaco-economic informa…