Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information
Role summary Build and run the operating engine of CSLs PPP ( Public-Private Partnerships ) Centre of Excellence — the governance, methodologies, data, systems and internal network that let CSL evaluate, decide on, and execute government
Questa posizione è in CSL Il processo di selezione sarà interamente gestito CSL. Questa opportunità è disponibile in Glattbrugg, Kgs. Lyngby, Barcelona, Munich, Mechelen, Rome, Paris, Ottawa, King of Prussia, Haywards Heath, Danderyd, Frankfurt, Milan. -
Responsibilities:• Manages and directs functions to comply with standard operating procedures, regulatory safety and pharmacovigilance and business technology quality standards in compliance with national and international regulations, such as relevant GxP guidelines and national and international
Role SummaryBuild and run the operating engine of CSLs PPP ( Public-Private Partnerships ) Centre of Excellence — the governance, methodologies, data, systems and internal network that let CSL evaluate, decide on, and execute government partnership
Responsibilities: You will be responsible for scientific input to clinical development strategies and therapeutic areas. Provide scientific and clinical development input for the safe and efficient execution of assigned programs, ensuring the highest quality and full
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables