Back to jobsRepresent independently Clinical Pharmacology and provide clinical pharmacology support and guidance to clinical stage project teams.
Lead the analysis, interpretation, integration and reporting of clinical pharmacology data
Conduct PK and PK/PD analyses to guide clinical development decisions
Provide clinical pharmacology input for regulatory submissions such as briefing documents, IND, CTA and NDA
Prepare and input independently appropriate documents or sections of clinical protocols, Investigator Brochures, Clinical Study Reports with respect to Clinical Pharmacology studies or data
Closely partner with Research, Bioanalytical, Clinical, Regulatory, Project Management, and other R&D functions
Preparation of abstracts and manuscripts for publications
Network with external expert consultants, CRO partners and academic sites to problem solve and develop scientific solutions to clinical pharmacology issues
