Quality in a globalized drug safety network is a matter of operational resilience as much as regulatory mandate. This role serves as aGVPAuditor within our Research & Development Quality audit program, responsible for executing the global
Role Overview The postholder will lead the design and execution of integrated, data-driven engagement strategies across digital and field channels for the UK & Ireland portfolio. They will partner with cross-functional teams including Brand, Medical, Compliance,
PV Systems & Process Lead Patient safety depends on pharmacovigilance systems that work and work well. In this role, youll be at the centre of keeping CSLs global PV system compliant, continuously improving, and inspection-ready across Global
GLP Vendor Oversight and QA Lead The integrity of nonclinical data depends on more than what happens inside a companys walls. Much of the critical work in GLP-regulated research safety studies, toxicology, analytical testing is carried
The Head of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs,
PV Systems & Process Lead Patient safety depends on pharmacovigilance systems that work — and work well. In this role, youll be at the centre of keeping CSLs global PV system compliant, continuously improving, and inspection-ready across
The Head of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs,