Biostatistics and Safety
656 open positions
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Principal Stats Programmer (VAX) SanofiHyderabad, IN 15d Lead statistical programming for clinical trials across the Vaccines R&D value chain, delivering CDISC-compliant data packages and integrated clinical databases for regulatory submissions and reporting.
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Biostatistician II ThermofisherShanghai, China 15d Lead statistician responsible for statistical aspects in the design and analysis of clinical trials, including project management, analysis, and report preparation.
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Biostatistical Programming Manager AmgenUnited States - Remote $129k–$175k15d Lead an FSP-based programming team conducting analyses supporting CfOR's Data & Analytic Center.
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Manager - Biostatistics, Epidemiology & Real-World Evidence↗ Carrot RecruitmentManchester Area, United Kingdom £52k–£56k15d Providing statistical and methodological expertise for real-world evidence (RWE) and observational research projects for pharmaceutical and biotechnology clients.
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Statistical Programmer↗ Connect Life Sciences 15d Statistical programmer managing clinical trial data conversion, analysis, and submission documentation for oncology studies.
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Associate Director, Biostatistics BristolmyerssquibbRemote $173k–$210k15d Lead biostatistician guiding design, execution, and interpretation of statistical analyses for oncology clinical trials to develop radiopharmaceutical therapies.
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Sr Principal Analyst, Statistical Programming BiibhrRemote $141k–$188k15d Lead and oversee statistical programming activities across clinical studies and programs, ensuring compliance with regulatory standards and driving data strategy.
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Clinical Data Scientist↗ ICON Strategic SolutionsReading, England, UK 15d Design, build, and maintain R Shiny applications for clinical study monitoring, data visualization, safety review, and exploratory analysis to support clinical development programmes.
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Principal Biostatistician FSP - Translational Medicine↗ CytelEstonia 15d Lead early development clinical studies and provide statistical expertise for translational medicine and clinical oncology projects across drug development stages.
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Epidemiology Medical Writing + Research Manager, RWLP (EMEA or LATAM - Remote Based)↗ Syneos HealthRemote 15d Managing Real World Evidence (RWE) research projects involving claims database analyses, observational studies, and patient-reported outcomes studies, with a significant focus on medical writing for protocols, reports, and publications.
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Senior Biostatistician EdwardsUSA - California – Irvine $119k–$168k15d Develop and execute Statistical Analysis Plans (SAPs), perform and validate statistical analyses, and support clinical study reports and regulatory submissions for transcatheter heart valve replacement studies.
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Associate Director, Biostatistics BmsRemote - United States - US $173k–$210k15d Lead biostatistician guiding the design, execution, and interpretation of statistical analyses for oncology clinical trials to develop radiopharmaceutical therapies.
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Lead Data Analyst↗ EPAM SystemsDesde casa, AR 15d Lead Data Analyst supporting a major pharmaceutical client's in vitro application portfolio by acting as a domain expert for a team of Full-Stack and Data Engineers.
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Director, Data Solutions TempusRemote 15d Senior scientific advisor and team leader designing real-world evidence analyses for biopharma partners to answer R&D and clinical development questions using multimodal clinical, molecular, and imaging data.
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Associate Director (m/f/x), Real World Evidence (RWE) Science CslSeqirus Netherlands - Amsterdam 15d Senior scientific leader driving global real-world evidence (RWE) strategies and study execution to support late-stage and marketed vaccine products.
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Experienced Feasibility Informatics Analyst MedpaceCincinnati, Ohio 15d Architect, mine, analyze, and visualize clinical trial data to inform study design choices and support proposal feasibility strategies for pharmaceutical development.
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Principal Statistical Programmer / Study Lead Programmer (R & CDISC)↗ DecskillLisbon, Portugal 16d Lead statistical programming for Phase III clinical studies, ensuring data quality and regulatory compliance via CDISC standards.
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Senior Director, Biometrics↗ Enanta PharmaceuticalsWatertown, MA, US $204k16d Lead the Biometrics organization to translate clinical data into rigorous statistical evidence for virology and immunology drug development.
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Senior Biostatistician (UK/Europe)↗ Worldwide Clinical TrialsRemote 16d Provide expert statistical leadership and consultancy across clinical projects and sponsor programmes, ensuring scientific rigour in study design, analysis, and reporting.
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Statistical Programmer↗ Adelphi GroupEngland, United Kingdom 16d Coordinate and provide analytical support for single-sponsor secondary data studies by conducting complex data manipulation and analysis of existing real-world data sources worldwide to meet clients' real-world evidence needs.
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Statistics Leader (Oncology)↗ GskStevenage, England, UK 16d Manage statistical planning and delivery across clinical programs in oncology, designing robust trials and analyses to shape development decisions and regulatory strategy.
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PLS R&D - Experienced Associate↗ PwC Acceleration Center IndiaBengaluru East, Karnataka, India 16d Support global consulting engagements for pharmaceutical, biotechnology, and life sciences organizations by conducting strategic analyses, transformation initiatives, and operational excellence projects across the R&D and commercial value chain.
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Associate Director, Oncology Outcomes Research AstraZenecaGaithersburg, Maryland, United States of America $151k16d Lead high-impact health outcomes and real-world evidence (RWE) programs to define medicine value and accelerate patient access.
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Clinical Pharmacology Principal Scientist↗ Business Solutions by TaketalentColmenar Viejo, Community of Madrid, Spain 16d Lead clinical pharmacology and model-informed drug development (MIDD) for innovative oncology therapies, generating PK/PD insights to optimize early clinical development and support regulatory decisions.
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Senior Manager, Statistical Programming↗ AgenusRemote, US 16d Develop, validate, and deliver high-quality clinical trial datasets, statistical analyses, and regulatory submission outputs for oncology clinical development programs.
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Sr. SDTM Programmer↗ BiogenRemote, US $90k–$117k16d Lead study-level SDTM programming activities to deliver annotated CRFs, specifications, datasets, define.xml, and Study Data Reviewer Guides for clinical trials.
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Senior Study Director - ADME Metabolite Identification LabcorpUSA - WI - Madison - 3301 Kinsman Boulevard 16d Managing the design, conduct, and reporting of ADME (Absorption, Distribution, Metabolism, and Excretion) studies with a specific focus on Metabolite Identification to meet scientific, regulatory, and client requirements.
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Scientist III, Clinical Regulatory Writing CardinalhealthIreland-FIELD 16d Author, review, and edit clinical regulatory documents (CSRs, protocols, CTD summaries) for pharmaceutical and biotechnology clients to ensure compliance with global regulatory requirements.
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Biostatistician 2 IqviaShanghai, China 16d Prepare analysis plans, write specifications for statistical outputs, interpret analyses, and author statistical sections of study reports for clinical trials.
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Senior Statistical Programmer/Analyst Consultant (Hybrid at NJ/PA) ClinChoiceUnited States 18d Senior Statistical Programmer delivering technical programming and information components for clinical studies and projects.
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Biostatistician / RWE Methodologist / Clinical Data Analyst↗ PromptlyRemote 19d Design and execute real-world evidence (RWE) studies using federated hospital data to generate clinical insights for pharmaceutical sponsors.
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?Senior Statistical Programmer↗ Durham, NC, US 19d Performs statistical and database programming for clinical projects to ensure data integrity, accuracy, and alignment with trial protocols and regulatory requirements.
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Biostatistician↗ LumanityLondon, ENG, GB 19d Executes statistical analyses of patient-centered outcomes (PRO/COA) endpoints for clinical trials, supporting EU Joint Clinical Assessment (JCA) submissions and regulatory dossiers.
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Associate Director, Biostatistics SumitomopharmaRemote $166k–$207k19d Statistical lead for clinical development programs, providing strategic input on study design, analysis, and regulatory submissions.
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Statistician↗ ReckittHR, IN 19d Provide expert statistical input and evidence generation for medical claims and product registration across the hygiene, health, and nutrition portfolio.
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Sr. Biostatistician UchicagoChicago, IL, US $70k–$110k19d Provides statistical guidance for designing and analyzing basic science, clinical, and population-based studies to support research proposals and publications.
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