Director, Clinical Pharmacology & Pharmacometrics (Remote)
Jazz Pharmaceuticals - London, London
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If you are a current Jazz employee please apply via the Internal Career site.Not sure what skills you will need for this opportunity Simply read the full description below to get a complete picture of candidate requirements.Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visitwww.jazzpharmaceuticals.comfor more information. Brief Description: This position is responsible for leading efficient, innovative, clinical pharmacology and/or PK/PD studies from phase 1 to phase 4 through working with cross-functional team members.Essential Job Functions:Job ResponsibilitiesDevelopment of the clinical pharmacology strategy of multiple programs spanning from candidate nomination for GLP toxicity studies through phase 4Support clinical study protocol (phase 1-4) development, PKPD data analysis/interpretation, and study reportServe as the clinical pharmacology Lead at cross function teams, and responsible for the dose selection and rationale in phase 1 studies and contribute to dose selections in clinical studies beyond phase 1Work with the pharmacometrics lead and relevant cross-function teams to plan and support PKPD modeling for internal or regulatory decision makingsContribute to the preparation of relevant sections of regulatory submissions including IND, and NDA/BLA documentsAddress queries from regulatory agencies during reviews and inspectionsIdentify and manage consultants and vendors supporting clinical pharmacology studiesContribute to the timely publication and/or presentation of clinical pharmacology and pharmacometrics dataRequired Knowledge, Skills, and AbilitiesPhD or MD with significant years of experience in clinical pharmacokinetic and pharmacokinetic-pharmacodynamic studies and data analysis/interpretationsStrong understanding of clinical pharmacology and pharmacometrics principles and the drug development processGood working knowledge of software for PK/PD analysis (e.g. Phoenix WinNonlin, R, ADAPT and NONMEM) Ability to work both independently and on strong cross functional teamsExperience in regulatory submissions and agency interactions related to INDs, CTDs, NDAs or BLAsExcellent written and oral communication skills including good presentation skillsCollaborative and flexible in personal interactions at all levels of the companyJazz Pharmaceuticals is an equal opportunity/affirmative action employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html.Remote working/work at home options are available for this role.
Created: 2025-09-08