NewStatistician Intern Bayer AGStatistician InternWhippany, NJ$20.75–$58.50 / hourThe successful candidate must be a high performer interested in the interactions between science and policy, eager to work with dynamic people and contribute to a changing environment; Candidates must be available for an assignment of up to three months at Bayer's Whippany, New Jersey, site from mid-May to mid-August 2027 (different options are available); Hybrid/home-based assignments will also be considered; For non-US citizens, as required by current immigration law, it is the student's responsibility to provide the appropriate documentation showing proof of eligibility to work and earn compensation in the United States. Bayer seeks an incumbent who possesses the following: Pursuing a Master's or PhD degree in Statistics, Biostatistics, or related fields from an accredited college/university; Must be motivated and well-organized; Strong analytical and quantitative abilities with excellent written and verbal communication skills; Strong proficiency in Microsoft Word, Excel, and PowerPoint; Good working knowledge of SAS, R, and/or Python; Ability to participate within a multi-disciplinary team as well as act autonomously, as appropriate.
Statistician Karwell TechnologiesStatisticianNewark, NJProvides general infrastructure support to the Department (presents / teaches at the department meetings, contributes to other general department documents or policies, assists with newsletter, helps in department libraries, or trains new hires). Supports the department by directly contributing to simple or moderately complex study protocols and bid defenses, including organizing teams and implementing strategies to ensure process and programming efficiencies.
Statistician Katalyst Healthcares & Life SciencesStatisticianNewark, NJProvides general infrastructure support to the Department (presents / teaches at the department meetings, contributes to other general department documents or policies, assists with newsletter, helps in department libraries, or trains new hires). Supports the department by directly contributing to simple or moderately complex study protocols and bid defenses, including organizing teams and implementing strategies to ensure process and programming efficiencies.
Senior Principal Statistician, Biometrics Ferring Pharmaceuticals, Inc.Senior Principal Statistician, BiometricsParsippany, NJ$191,000–$225,000 / yearResponsibilities: Evidence generation and real-world evidence (RWE) Supporting the design, conduct, analysis and reporting of RWE studies Contribute to integrated evidence generation strategies combining clinical trial and real-world data Supporting use of RWE in regulatory submissions, health technology assessment (HTA), and lifecycle planning Clinical development and statistical contribution Providing statistical input to clinical development plans and target product profiles Authoring statistical analysis plans and contributing to study design Supporting analysis and interpretation of clinical trial data Contributing to clinical study reports and regulatory submissions Assessment of business development opportunities Critically review and evaluate clinical trial data to assess efficacy, safety, and asset value, including opportunities for life cycle management such as label expansion, new indications, and geographic growth. Requirements: Bachelor’s degree required, Master’s degree or PhD in Statistics, Biostatistics, or a related quantitative field preferred 5+ years of experience working in the pharmaceutical industry· Proficiency in statistical programming languages (e.g., R, SAS)· Experience working with registry/claims data, including assessing the suitability and quality of such data sources in accordance with FDA guidance, and applying methodologies for analyzing observational data, e.g.
NewSenior Research Statistician - Statistical Innovation Hybrid AbbVie IncSenior Research Statistician - Statistical Innovation HybridFlorham Park, NJThe Senior Research Statistician in Statistical Innovation is responsible for providing scientific and statistical leadership to support initiatives on designing innovative clinical trials and to evaluate, develop and deploy advanced and novel statistical/analytical modeling and simulations to drive statistical innovation modeling and simulation in Clinical Development. Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position.
Senior Medical Director/Medical Director, Clinical Trial Lead KardiganSenior Medical Director/Medical Director, Clinical Trial LeadPrinceton, New Jersey$242,000–$347,000 / yearThe Senior Director / Medical Director - Clinical Trial Lead will be a physician with extensive drug development expertise who will be expected to lead to the clinical development strategy for the phase 1-3 clinical trials of the program, including the protocol design, operational planning and trial execution, medical and safety monitoring, trial close out, trial results interpretation, and preparation for dissemination of the trial results, working with academic partners. Takes primary responsibility for the clinical development function, working with statisticians, modelers, and project team-members, for contributing to the creation of trial-specific statistical analysis plans, and for the interpretation, reporting, and dissemination of the final results, working closely with academic partners.
Senior Scientist, Biostatistics, Clinical Safety Statistics Merck & Co IncSenior Scientist, Biostatistics, Clinical Safety StatisticsRahway, NJ$117,000–$184,200 / yearInteract with members of cross-functional safety teams (e.g., Safety Physicians and Scientists, Clinical Trial Physicians and Scientists, Epidemiologists, Regulatory Liaisons, Early and Late Development Statisticians, Statistical Programmers, and others) on the planning and execution of ongoing safety evaluations for products across pre-marketing and post-marketing development stages. Quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health.