About usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years of experience, operating in 31 countries with more than 7,000 employees (Chiesi Group). To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group researches, develops, and markets innovative drugs in its main therapeutic areas: Discover more here.We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, recognizing high social and environmental standards. We are a reliable company that adopts and promotes transparent and ethical behavior at all levels.We believe that the success of Chiesi is built and shaped by our people and our shared Values and Behaviors. Our people make a critical difference to our success, which is why attracting and retaining the right talent is vital. We aim to enrich our culture by living and breathing our values and behaviors.In fact, we are a global family made up of different cultures, genders, generations, ethnicities, abilities, sexual identities, and many other enriching diversities.Chiesi Research DevelopmentOur RD team is a fundamental asset, divided into functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical development, regulatory affairs, pharmacovigilance, intellectual property, quality assurance, RD project and portfolio management. Headquartered in Parma (Italy), the team also operates in Paris (France), Chippenham (UK), Cary (US), Stockholm (Sweden), Toronto (Canada), and Shanghai (China).Who we are looking forPurposeThe candidate will contribute to defining the Model Informed Drug Development strategy across projects for various therapeutic indications and data types to optimize future studies. They will be responsible for ensuring the delivery of study results within specified timescales and quality standards, complying with Chiesi SOPs and standards, and supporting Chiesi Group objectives. The Modelling and Simulation Scientist Expert provides advanced modeling skills to multiple projects, working within a dedicated team and with external experts to support analysis delivery, enhance project impact, and develop quantitative methodologies.Main ResponsibilitiesLead pharmacometrics activities including PK, PK/PD, and PBPK modeling, simulation, and reporting for multiple projects.Assist senior management in selecting action plans aligning with drug development objectives; contribute to MIDD strategy for global biopharmaceutical development.Perform hands-on pharmacometric activities within clinical development programs using relevant software (e.g., NONMEM, Monolix, R, MATLAB).Establish and maintain strategic CRO interactions, managing communications, publications, and plans.Author, review, or approve pharmacometrics reports and regulatory document sections; participate in meetings with clients and regulatory agencies as needed.Experience RequiredAt least 3 years in similar roles.EducationScientific degree, Doctorate in pharmacometrics, clinical pharmacology, pharmaceutical sciences, medicine, statistics, chemical engineering, or related fields.LanguagesEnglish FluentTechnical SkillsLeadership in Pharmacometrics, biostatistics, and PK/PD activities. Experience with population PK and PK/PD modeling software (NONMEM, Monolix, R, MATLAB).Soft SkillsCommunication skillsProblem solvingTeam workingLearning agilityWhat we offerJoin a dynamic, fast-growing, friendly environment. We invest in continuous training, learning, and development, promoting a positive work environment and work-life balance. We offer flexible working, remote options, relocation support, tax assistance for foreign colleagues, and other people-care services.
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