Biostatistics and Safety
403 open positions
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Manager - Exploratory Analysis (Hybrid) AbbVieNorth Chicago, IL, us 1d Provides statistical expertise to support drug discovery, target identification, and clinical biomarker exploration for precision medicine, enabling objective decision-making across the drug development lifecycle.
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Sr. Scientist, Stat. Programming MsdCHE - Zurich - Zurich (The Circle), CH 1d Develop statistical programming activities to create analysis datasets, tables, listings, and figures for Health Technology Assessment (HTA) dossiers from clinical trial data.
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Sr Biostatistician II ThermofisherBangalore, India 1d Lead statistician and project lead delivering statistical analysis, protocol design, and reporting for complex clinical trials and NDA projects.
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Senior Statistical Programmer SanofiHyderabad, IN 1d Implement statistical analysis plans and provide QC'd data packages (tables, figures, listings) for publications and ad-hoc analysis requests.
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Senior Biostatistician II VrtxBoston, MA, US $132k–$132k2d Designs, develops, and executes statistical infrastructure for clinical trials, observational studies, and real-world data investigations in drug development.
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Principal Statistical Programmer IqviaDurham, North Carolina, United States of America $98k–$98k2d End-to-end statistical programming for clinical studies from setup through regulatory submission, ensuring CDISC compliance and high-quality deliverables.
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Associate Director, Safety Epidemiology – Global Patient Safety AstraZenecaUK - Luton 2d Lead end-to-end delivery of complex post-authorisation safety studies (PASS) and generate epidemiological insights using real-world data to inform regulatory decision-making and benefit-risk assessments for AstraZeneca products.
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Biostatistician GeisingerRemote 2d Provide statistical support, design study plans, and analyze data for clinical and research investigators.
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Associate Director, TAIP Principal Analyst - Trial Analytics, Insights & Planning (TAIP) BristolmyerssquibbWarsaw-WeWork-PL $392k–$392k2d Own study-level analytics planning and delivery from protocol concept through execution for global clinical trials, leading a team of 3–5 analysts to translate study objectives into analytical workstreams.
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Temp - Director Pharmacoepidemiology RegeneronRemote - United States 2d Develop and implement pharmacoepidemiology strategy for real-world evidence (RWE) and regulatory agency-required epidemiologic studies to support clinical development and regulatory filings.
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Associate Director, Epidemiology BiibhrRemote $176k–$176k2d Provide epidemiologic expertise (conceptual, methodological, statistical) to support decision-making, program development, and regulatory requirements across Safety, Clinical Development, and Medical functions.
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Senior RWE Research Analyst NovartisHyderabad (Office), IN 2d Lead scientific design, protocol development, and methodological oversight for observational database analytics and Real-World Evidence (RWE) projects, translating findings into actionable insights for medical affairs stakeholders.
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Vice President, Biostatistics 4dmoleculartherapeuticsRemote $330k–$330k2d Enterprise-level strategic statistical leadership and oversight for global drug development programs, driving quantitative decision-making and regulatory strategy.
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Principal Statistical Programmer ImmunomeincBothell, WA Headquarters $154k–$154k2d Senior technical expert developing, validating, and delivering high-quality SAS programming deliverables for clinical trial analysis and regulatory submissions.
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Principal Scientist, PSSM ARD, GMP Analytics, Stability Strategy & Operations PfizerUnited States - Connecticut - Groton $106k–$106k3d Lead the development and communication of scientifically sound stability strategies for drug substance and drug product programs to support new medicine development and registration.
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Global Medical Development Manager↗ SandozTS, IN 3d Provides medical development input, patient safety oversight, and clinical context evaluation for generic and biosimilar product development to enable scientifically justified strategies.
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Associate Director, Real World Biostatistics GskUSA - Pennsylvania - Upper Providence 3d Lead strategic initiatives for value delivery by applying advanced biostatistical methods and AI tools to real-world data (RWD) to generate real-world evidence (RWE) for trial design, regulatory submissions, reimbursement, and safety signals.
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Assoc Director, Statistical Programming GileadUnited States - California - Foster City $196k–$196k3d Lead statistical programming and analysis for clinical study reports and regulatory submissions in oncology, hematology, virology, and inflammation.
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Senior Statistician, CVRM RocheSouth San Francisco, US $137k–$137k3d Senior Statistician leading statistical design, conduct, analysis, and interpretation of clinical trials to ensure scientific rigor and regulatory compliance for drug development.
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VP, Biometrics AbCelleraRemote $0k–$0k3d Lead biometrics across the full drug development lifecycle (IND to post-approval) for antibody-based medicines, building a world-class function from the ground up.
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Scientific Medical Writer↗ Well Health Technologies CorpRemote $75k–$75k4d Design and write clinical study protocols, informed consent forms, and regulatory documents for Phase 1-IV and bioequivalence studies.
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Senior Clinical Statistical Programmer (Portfolio Development / Biometrics / Programming) CslEMEA, GB, Berkshire, Maidenhead, CSL Behring 4d Lead end-to-end statistical programming for clinical trials from setup to regulatory submission, ensuring data integrity and audit readiness.
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Senior Statistical Programmer – CDISC Lead MyhrabcWEMEA > Spain > Remote 4d Senior Statistical Programmer acting as a Subject Matter Expert (SME) and Project Manager for CDISC-compliant statistical programming, leading the preparation, execution, and documentation of regulatory submission data packages.
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Global R&D Risk and Compliance Manager Gsknch2 Locations 4d Ensure compliant organization and robust inspection readiness for R&D functions through risk oversight, governance, and management monitoring.
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Analista de protocolo Trainee II QimaAparecida de Goiânia, GO, br 4d Designing bioequivalence/bioavailability study protocols, managing clinical unit pharmacy operations, and supporting regulatory submissions for life sciences research.
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Senior / Principal Analyst, Statistical Programming↗ Simulstat IncRemote 5d Generate SDTM and ADaM specifications, datasets, reviewer's guides, and define.xml files; develop and validate SAS and/or R programs for clinical trial data reporting.
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Sr. Manager, Medical Affairs - Evidence Generation and Data Insights InsuletActon, Massachusetts, US $156k–$156k5d Lead global real-world evidence (RWE) generation and provide biostatistical support for clinical trials to support the development and commercialization of diabetes management products.
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R&D Engineer I_Product AbbottChina > Hangzhou : #198 12th Street, Hangzhou Economic & Technological Development Area 5d Support R&D projects by developing experimental plans, ensuring design robustness and reliability, managing design controls, and preparing technical documentation for regulatory submissions and product transfers.
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Biostatistician (Neurology) JhuRemote $57k–$57k5d Analyze large-scale longitudinal data from electronic health records and clinical databases to support neurology research and clinical trials.
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