A prominent pharmaceutical group with a broad and diversified product portfolio Reports to Head of Regulatory Affairs Role focused on submission and communication with regulators Summary We are partnering with a prestigious pharmaceutical group to recruit
A prominent pharmaceutical group with a broad and diversified product portfolio Reports to Head of Regulatory Affairs Role focused on submission and communication with regulators Summary We are partnering with a prestigious pharmaceutical group to recruit
Primary Responsibilities Non-clinical development strategy and execution For in vivo gene editing pipelines (e.g., liver targeting, ophthalmology, central nervous system, etc.), independently develop and lead high-quality non-clinical pharmacology, pharmacokinetics, and toxicology study strategies in full compliance