Biostatistics and Safety
646 open positions
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Epidemiology Analyst AmgenIndia - Hyderabad today Conducts observational research using real-world data to support drug development, registration, and commercialization by characterizing disease incidence/prevalence, safety, and treatment patterns.
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Lead Biostatistician (IVD Analytical) NateraUS $144k–$180ktoday Lead biostatistics efforts for designing, analyzing, and interpreting R&D and analytical validation studies for complex biomarkers used in cancer screening, monitoring, and management.
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Associate Director, Statistics - Immunology (Hybrid) AbbVieSouth San Francisco, CA, us today Provide statistical leadership for clinical development and life-cycle management strategies, including clinical trials, patient safety, and global medical affairs.
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Biostatisticien H/F QimaNice, Provence-Alpes-Côte d'Azur, fr €35ktoday Analyze clinical studies to support decision-making for the Director of Clinical Studies and the clinical research team.
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Senior Statistical Scientist SobiBasel, BS, ch 1d Lead statistical analyses, study design, and regulatory submissions for clinical studies in the pharmaceutical industry, ensuring compliance with SOPs and guidelines.
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Statistical Programmer SystImmuneUSA $80k–$100k1d Develop and validate SDTM and ADaM datasets, tables, figures, and listings for clinical trial analyses and regulatory submissions.
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Principal Statistical Programmer Pharpoint ResearchUSA $88k–$128k1d Oversee biostatistics programming activities, including development of analysis datasets and statistical summaries, ensuring timely, accurate, and efficient delivery in line with GCP and applicable SOPs.
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Associate Director, Biostatistics BmsPrinceton - NJ - US $190k–$264k1d Associate Director of Biostatistics leading cross-functional development teams in trial design, protocol development, analysis planning, and regulatory submissions for clinical assets.
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Biostatistician-P2 BostonscientificMaple Grove US-MN, United States | N/A $72k–$136k1d Support clinical trials through statistical analysis, programming, and data interpretation to support scientific decision-making and medical device safety evaluation.
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Client Dedicated Lead Statistician - Medical Affairs, FSP ThermofisherBoston, Massachusetts, USA $135k–$175k1d Design and implement statistical methodologies for complex clinical trials and research projects in autoimmune disease, providing strategic guidance on study design and analysis.
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Associate Director, Precision Medicine BristolmyerssquibbCambridge Crossing - MA - US $209k–$254k1d Leads the development and implementation of the Model-Informed Drug Development (MIDD) strategy for drugs in clinical development, integrating diverse data through pharmacometric (PMx) models to inform regulatory decision-making.
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Associate Principal Scientist (Associate Director) - Outcomes Research MsdUSA - New Jersey - Rahway $157k–$247k1d Planning and managing real-world and economic evidence activities for inline and pipeline products to support value evidence needs of clinicians, payers, policymakers, and health systems globally.
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Director Biostatistician↗ Asahi Kasei TherapeuticsStockholm, Stockholm County, Sweden 1d Strategic statistical lead for clinical development programs, ensuring statistical rigor, consistency, and quality across studies while guiding study designs and methodologies.
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Principal Statistical Programmer Consultant ClinChoiceRemote 2d Lead statistical programming for solid tumor oncology clinical trials, developing datasets and reports for regulatory submissions.
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Health Economic Modeler↗ Analysis GroupLondon Area, United Kingdom 2d Build health economic models (cost-effectiveness, budget impact) to demonstrate value for life sciences products and support regulatory/HTA submissions.
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Associate Director, SAS Programming Acadia-Pharmaceuticals-IncRemote $163k–$203k2d Lead statistical programming for assigned compounds, ensuring CDISC conformance, submission readiness, and quality of deliverables produced internally or by partners.
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Principal Statistical Programmer ImmunomeincBothell, WA Headquarters $154k–$178k3d Senior technical expert developing, validating, and delivering high-quality SAS programming deliverables for clinical trial analysis and regulatory submissions.
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Senior Specialist Product Regulatory (m/w/d) Basf-SeLimburgerhof, RHEINLAND_PFALZ 3d Evaluate the safety of pesticide and biocide active substances and plant protection products for humans, ensuring sustainability and compliance with highest safety standards.
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Sr. Data Scientist, Assay Development DELFI Diagnostics, Inc.Palo Alto, CA 3d Design studies and analyze data to evaluate assay performance, inform product decisions, and support regulatory submissions for early cancer detection blood tests.
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Sr. Associate,Toxicology ScjUSA - WI - Racine 4d Lead and guide technical teams in shaping human health toxicology strategy, conducting risk assessments, and overseeing laboratory studies to ensure product safety and regulatory confidence.
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Epidemiology Forecasting, Associate Director VrtxRemote $172k–$258k4d Develop scientifically rigorous global estimates of disease incidence, prevalence, and population size to inform drug development, commercial planning, and regulatory filings.
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Senior Manager, Statistical Programming↗ EisaiNutley, NJ, US $139k–$182k4d Manage statistical programming projects from inception through submission, developing and reviewing SAS code to create datasets and summary Tables, Graphs, and Listings (TLGs) per Statistical Analysis Plan.
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Programmer Analyst II↗ Thermo Fisher ScientificKA, IN 4d Bioinformatics programming supporting statistical and computational needs of clinical research projects, delivering reliable clinical research data and outputs.
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Feasibility Informatics Analyst↗ MedpaceMünchen, BY, DE 4d Architect, mine, analyse, and visualise clinical trial data to inform study design choices and support proposal feasibility strategies.
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Utredare preklinik↗ Medical Products Agency LäkemedelsverketUppsala, Uppsala County, Sweden 4d 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–£37k4d 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–£40k4d 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 4d 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 4d Develop advanced kinetic models and compare frequentist and Bayesian statistical performance for predicting the stability of biological products.
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Assessor/-in (m/w/d) Qualitätsbewertung Paul-Ehrlich-Institut Bundesinstitut für Impfstoffe u. biomedizin. ArzneimittelLangen (Hessen), HESSEN 5d Evaluate quality data for blood products and gene therapy drugs during European and national approval processes.
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Director, Statistical Programming AstraZenecaWaltham, Massachusetts, United States of America 5d Lead statistical programming for Phase 1/2 oncology clinical trials, managing a team of programmers to deliver high-quality data products for regulatory submissions.
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Support Epidemiologist (Medical Device Active Surveillance Program)↗ Tunnell Government ServicesSilver Spring, MD, US 5d 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 5d 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 5d 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 5d 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 5d 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 5d 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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