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Senior Statistician Beerse Belgium,  

Posted on : 15 April 2017

Project Description

Janssen Research & Development, LLC, a Johnson and Johnson Company, a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Statistician. Janssen Research & Development develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious diseases, diabetes, hematology, metabolic disorders, immunologic disorders, and reproductive medicine. The Quantitative Sciences organization integrates Clinical and non-Clinical Biostatistics, Clinical Pharmacology, and Model Based Drug Development in a single aligned organization as part of Janssen Research & Development. We work in cross-disciplinary Quantitative Sciences teams and apply quantitative principles across the R&D portfolio to enable optimal decision-making at the earliest time point and in the most efficient manner. We are specifically looking for a Senior Statistician to work in the Clinical Biostatistics Late Development group. The disease areas that are targeted are HIV, hepatitis, influenza and RSV. The candidate should be able to gain a thorough understanding of the safety, efficacy, the pharmacokinetics and the pharmacodynamics of one or more investigational compounds. He/she will be involved in the design, set-up and analysis of the clinical trials in close collaboration with other clinical team members. The team is looking for a candidate who has the ability to understand and apply innovative designs and analysis methods and supporting their evaluation via analytical studies and other appropriate methods. Knowledge in regulatory submissions is required.QualificationsCandidates not meeting one or more of below requirements will still be considered provided unique expertise in one or more relevant areas can be demonstrated. Ph.D. in Statistics or related field with about 2 years of relevant experience, or Masters in Statistics or related field with at least 5 years of relevant experience. Experience with antiviral drug development is a preProficient in SAS or R programmingBasic knowledge of regulatory guidance documents such as ICH guidanceExperience in developing clinical trial protocolsExperience producing clinical biostatistics top line reportsAbility to provide critical input to the statistical lead or team in optimizing study or trial designs in line with study or trial objectivesAbility to support scenario simulations and sample size calculations based on relevant technical and disease/scientific/functional area knowledgeGood written, oral, and interpersonal communication skillsAbility to work independentlyAbility to provide guidance, oversight and review of work performed by External Service ProvidersAbility to work effectively in a multidisciplinary team environmentFluency in English, both written and spokenWhat s in it for you &? Caring for the world, one person at a time & As an employee we consider you as our most valuable asset. We take your career seriously.As part of a global team in an innovative environment your development is key and our day-to-day responsibility. Through e-university, on the job training, various projects and programs, we ensure your personal growth.Our benefits make sure we care for you and your family now and in the future. Primary LocationBelgium-Antwerp-BeerseOrganizationJanssen Pharmaceutica N.V. (7555)Job FunctionR&DRequisition ID1700160710W


Beerse Belgium

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