Biostatistics and Safety
653 open positions
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Principal Biostatistician - Safety (FSP)↗ Thermo Fisher Scientific 5d Principal Biostatistician supporting clinical research programs for a biotechnology company developing therapies for autoimmune diseases and oncology, focusing on safety, regulatory reporting, and statistical analysis.
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Utredare preklinik↗ Medical Products Agency LäkemedelsverketUppsala, Uppsala County, Sweden 5d Evaluate data from pharmacological, toxicological, and ecotoxicological studies in applications for human and veterinary medicinal product approvals.
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Research Assistant in Medical Statistics/Research Associate in Medical Statistics↗ The University of SheffieldSheffield, England, UK £32k–£37k5d Provide statistical analysis, design input, and reporting support for clinical trials and research projects within the Division of Population Health.
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Research Assistant in Medical Statistics/Research Associate in Medical Statistics↗ University of SheffieldSheffield, ENG, GB £33k–£40k5d Provide statistical analysis, design, and reporting support for clinical trials and research projects within the Division of Population Health.
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Senior Consultant - Evidence Synthesis (Global Health Economics Team) - United Kingdom/European Union IqviaLondon, United Kingdom 5d Senior technical lead for evidence synthesis projects, conducting meta-analyses, indirect treatment comparisons, and network meta-analyses for healthcare clients.
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stage 6 mois mathématiques appliquées et modélisation SanofiMarcy-l'Etoile, FR 5d Develop advanced kinetic models and compare frequentist and Bayesian statistical performance for predicting the stability of biological products.
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Statistical Programming Strategy & Portfolio Lead, Associate Director AstraZenecaSweden - Gothenburg 6d Provide strategic programming leadership, planning, and project management for clinical drug development programs within the Cardiovascular Renal Metabolism (CVRM) Biometrics team.
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Assessor/-in (m/w/d) Qualitätsbewertung Paul-Ehrlich-Institut Bundesinstitut für Impfstoffe u. biomedizin. ArzneimittelLangen (Hessen), HESSEN 6d Evaluate quality data for blood products and gene therapy drugs during European and national approval processes.
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Support Epidemiologist (Medical Device Active Surveillance Program)↗ Tunnell Government ServicesSilver Spring, MD, US 6d Translates complex epidemiological and statistical analyses into clear, actionable presentation materials and records to inform the full lifecycle of medical device active surveillance activities.
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Principal Statistician↗ Warman O'BrienRemote 6d Lead biostatistics and programming activities for moderate-complexity clinical studies from planning to delivery.
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Supply Chain Lead - Chemistry Manufacturing and Controls↗ ZsBuenos Aires, Buenos Aires Province, Argentina 6d Lead decision analytics projects for pharmaceutical CMC development, serving as a subject matter expert on drug substance and drug product manufacturing to guide client and ZS team decision-making.
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Real World Evidence Expert↗ VRS RecruitmentRemote 6d Lead the design, execution, and delivery of global Real World Evidence (RWE) studies from concept through to publication to support regulatory studies and innovative medicine development.
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VP, Biostatistics↗ Biocryst Pharmaceuticals, Inc.Chiasson Office, New Brunswick, Canada 6d Planning and delivery of statistical activities to support the design, conduct, and analysis of clinical development studies and regulatory submissions.
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Pharmacometrician Scientist↗ ChemoAzuqueca de Henares, Castile-La Mancha, Spain 6d Provide technical and scientific support for NME and complex generic development projects by building mathematical models describing formulation effects on drug absorption and developing predictive PK models.
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Principal Biostatistician - Medical Affairs (FSP) ThermofisherRemote, France 6d Provide strategic statistical expertise and oversight for clinical research programmes, including Phase IIIb/IV trials, observational studies, and patient registries to support evidence generation for severe autoimmune disease therapies.
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Manager, Biostatistics PfizerUnited States - Massachusetts - Cambridge $106k–$177k6d Provide statistical support for clinical trial design, analysis, and regulatory submissions in the Inflammation and Immunology disease area.
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Lead Biostatistician - late-stage drug development↗ Vgs Rpo ServicesRemote 6d Lead statistical strategy for pivotal Phase II/III and late-stage clinical trials, influencing study design and supporting regulatory submissions for drug approvals.
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Supply Chain Lead - Chemistry Manufacturing and Controls↗ Zs AssociatesBuenos Aires, B, AR 6d Lead decision analytics projects for pharmaceutical CMC development, serving as a subject matter expert on drug substance and drug product manufacturing.
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5. Biostatistical Programming Assoc Dir↗ AmgenRemote 6d Lead global statistical programming for oncology and other therapeutic areas, ensuring submission and inspection readiness for large-scale clinical studies.
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PK Scientist I↗ AltasciencesLaval, QC, CA 6d Gather and synthesize scientific information, perform PK and TK analysis, and prepare high-quality documents to support sponsors' research programs.
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Modelling and Simulation PK/PD Expert AstraZeneca ABGöteborg, Sweden 6d Design and oversee complex preclinical studies using mathematical modelling to predict human pharmacokinetics/pharmacodynamics and inform dosing strategies for cardiovascular, renal, and metabolic disease treatments.
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Mid-Senior Statistical Programmers↗ Noymed CroRemote 7d Deliver statistical programming solutions for clinical trials, developing validated programs and macros to produce SDTM/ADaM datasets and TLGs.
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Lead Statistician↗ Morgan Prestwich - Global Biotech, Medtech & Cdmo RecruitmentLondon Area, United Kingdom 7d Lead statistical strategy and activities for a pivotal rare disease programme from study design through to BLA/MAA regulatory submission.
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Manager, Real World Evidence Science↗ CslKirkland, Quebec, Canada $134k–$159k7d Manage and provide technical expertise for Phase IV real-world evidence research across the influenza vaccine portfolio, including study development, coordination, and execution focused on epidemiology, vaccine effectiveness, and safety.
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Director Epidemiology Japan GskJapan - Tokyo - Akasaka 7d Lead the design and delivery of epidemiology and real-world evidence strategies to support medicine development in Japan.
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Research Associate↗ University of StrathclydeGlasgow, SCT, GB £38k–£47k7d Lead the delivery of a regulatory science project to develop and validate paediatric-specific TIM protocols coupled with mechanistic physiologically based pharmacokinetic (PBPK) modelling for predicting oral drug performance.
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Senior Clinical Pharmacologist AbbVieSan Francisco, CA, us 7d Conceive and execute novel scientific research and development in Clinical Pharmacology and Pharmacometrics (CPPM), generating PK/PD proposals and optimizing methods to support clinical development.
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Study Director / Technical Assistant - Non-clinical Toxicity studies EurofinsBengaluru, KA, in 8d Lead non-clinical toxicity studies ensuring GLP compliance, administering test items, and managing data/reporting for regulatory submissions.
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Scientist↗ A2-AI LLCAnn Arbor, MI, US $50k–$80k8d Collect, analyze, and interpret confidential nonclinical and clinical data to support clients' drug development programs using model-informed technical solutions.
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Study Design Statistician (Remote - Canada)↗ MmsRemote 8d Lead the full life cycle of KerusCloud support and statistical services, assisting customers with study design simulation and providing statistical consultancy to sponsors across clinical development.
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Sr Statistical Programmer, Oncology↗ Connect Life SciencesToronto, Ontario, Canada 8d Senior statistical programmer responsible for clinical data preparation, analysis, and submission using CDISC standards in oncology clinical trials.
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?Senior Statistician↗ Remote 8d Principal quantitative and statistical authority for the CLEAR project, overseeing advanced meta-analytic models, effect size computations, and statistical audits across evidence review streams.
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Stats Programmer↗ R&d PartnersManchester, England, UK 8d Analyze patient-reported outcome (PRO) data from clinical trials and observational studies to develop measures improving healthcare decisions.
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