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
Description Summary: The Associate Director PK is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK), toxicokinetic (TK), strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas. The Sr. Expert will
The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting,and regulatory interactions