Principal Investigator / Sr. Principal Investigator, Clinical Pharmacology & Pharmacometrics Incyte CorpPrincipal Investigator / Sr. Principal Investigator, Clinical Pharmacology & PharmacometricsWilmington, DEDemonstrated a general understanding of general DMPK disciplines in vitro ADME pharmacokinetics transporter DDI translational modeling biotransformation biomarker strategy is a plus Demonstrated publication record leadsenior author contributions is a plus Ability to prioritize and manage multiple projects while meeting project deadlines. Through the discovery development and commercialization of proprietary therapeutics Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology Oncology and Inflammation and Autoimmunity Headquartered in Wilmington Delaware Incyte has operations in North America Europe and Asia.
Associate Director, Quantitative Systems Pharmacology GSK plcAssociate Director, Quantitative Systems PharmacologyCollegeville, PA$151,500–$252,500 / yearAs an Associate Director of Quantitative Systems Pharmacology (QSP) Expert, you will develop and apply QSP models to guide clinical study designs and mechanistic interpretation of study results in support of development of treatments and combination of treatments for a variety of diseases and therapeutic areas. This role requires a highly motivated individual to develop and apply QSP models to guide clinical study designs and mechanistic interpretation of study results in support of development of treatments and combination of treatments for a variety of diseases and therapeutic areas.
Director, Clinical Pharmacology Madrigal Pharmaceuticals IncDirector, Clinical PharmacologyConshohocken, PA$228,074–$264,393 / yearThis individual will be responsible for developing integrated clinical pharmacology strategies that support dose selection, characterization of pharmacokinetics, pharmacodynamics, exposure-response characterization, intrinsic and extrinsic factors, drug-drug interactions, cardiac safety, special populations, and regulatory submissions. The successful candidate will collaborate closely with Clinical Development, Translational Medicine, Biostatistics, Regulatory Affairs, Medical Writing, and external partners to deliver high-quality Clinical Pharmacology strategies that enable informed development and regulatory decision making.