Biostatistics and Safety
415 open positions
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Associate Principal Scientist, Statistical Programming MsdRemote $145k–$145k4d Lead statistical programming for late-stage drug and vaccine clinical development, managing complex analysis datasets and regulatory submissions from individual trials to global applications.
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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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Programming, Statistics & Data Science (Multiple Roles) Industrial Placement, 2027 GskUK – London – New Oxford Street $29k–$29k4d Support professional statisticians and clinical research teams in study design, clinical trial programming, data analysis, and statistical innovation for drug development.
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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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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 Statistician II AstraZenecaUS - Durham - NC $120k–$120k4d Senior statistician providing statistical expertise for complex design, interpretation, and regulatory submissions for preclinical and clinical programmes in the pharmaceutical industry.
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Senior Director, Pharmacokinetics↗ IqviaRemote 4d Strategic, scientific, and operational leadership for Clinical Pharmacology PK/PD, Early Clinical Development Biostatistics, and Statistical Programming functions.
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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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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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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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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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Biostatistics Mgr ThermofisherRemote 5d Lead statistician responsible for statistical aspects of clinical trials from design through analysis and reporting, ensuring data integrity for new product introductions and ongoing research.
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Senior Principal DSX Data Scientist↗ RocheMississauga, ON, CA $149k–$195k5d Design and evolve next-generation statistical computing platforms, automate programming workflows, and create reusable coding macros to streamline evidence generation in clinical development.
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Manager, Statistical Programming GileadUnited States - California - Foster City $147k–$147k6d Lead statistical programming and analysis to produce high-quality datasets, tables, figures, and listings for regulatory study reports and integrated summaries.
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Senior Research Scientist - Real World Evidence PrecisionmedicinegroupRemote $100k–$100k7d Design and execute Real World Evidence (RWE) studies to improve healthcare outcomes by analyzing primary and secondary data for clients in the pharmacy and biotech sectors.
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Senior Research Scientist - Real World Evidence PrecisionaqRemote $100k–$100k7d Design and execute Real World Evidence (RWE) studies to improve healthcare outcomes by analyzing primary and secondary data for clients in the pharmacy and biotech sectors.
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Senior Scientist AmgenUnited States - Remote 8d Plan, manage, and monitor in vivo nonclinical safety studies for oncology, inflammation, general medicine, and rare disease therapeutic areas.
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Principal Programmer↗ PhastarRemote 8d Lead programming for clinical and non-clinical studies, producing and validating datasets for regulatory submissions while adhering to CDISC SDTM and ADaM standards.
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Head of Biorisk and Compliance CrickLondon $78k–$78k8d Lead the Institute's approach to biorisk management, regulatory compliance, and assurance for complex biological research.
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Staff GMP Statistician RegeneronRENSS - GLOBAL VIEW, US $103k–$103k8d Lead strategic statistical deployment, root cause analysis, and process improvement to accelerate drug development and approval using advanced modeling in a GxP environment.
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Clinical Scientist↗ Ocugen Opco IncMalvern, PA, US 8d Clinical scientist supporting retina development programs by analyzing clinical trial data, generating visualizations, and informing study execution and development strategy.
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Director Respiratory Bioequivalence Strategy Lead ViatrisSandwich, England, United Kingdom 8d Leads bioequivalence strategy for respiratory product development programs to ensure regulatory compliance and optimize in-vivo performance.
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Principal Statistical Programmer /Analyst Consultant -CVRM ClinChoiceUK 8d Lead statistical programming activities for clinical trials, developing SAS programs and datasets, and supporting regulatory submissions.
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Senior Statistical Programmer-Philippines InderoRemote 9d Lead statistical programming for clinical trials, developing and validating CDISC-compliant datasets (SDTM, ADaM) and TLFs for regulatory submissions.
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Senior Biostatistician CareDxRemote $112k–$112k9d Apply statistical techniques to design, analyze, and report on clinical studies for solid organ transplantation diagnostics products.
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Scientist, CMC Quantitative Sciences ModernaTXNorwood, Massachusetts 9d Scientist applying statistics, data science, machine learning, and mechanistic modeling to solve scientific and operational problems across product, process, and platform lifecycles in CMC.
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サRegulatory Publishing Manager (LATAM)↗ サイネオス・ヘルスRemote 9d Leading the creation, assembly, and publishing of electronic regulatory submissions to global health authorities for a portfolio of drug development programs.
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Senior Research Statistician - Immunology (Hybrid) AbbVieNorth Chicago, IL, us 9d Provide statistical support for clinical trials and scientific research studies to advance medicines for patients.
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Study Director – Toxicology EurofinsBengaluru, KA, in 10d Designing, conducting, overseeing, and reporting non-clinical safety studies (GLP and non-GLP) to support drug development and regulatory submissions.
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Senior RWE Biostatistician↗ FortreaEstonia 10d Lead design, analysis, and interpretation of non-interventional and Real-World Evidence (RWE) studies for global pharmaceutical and biotechnology clients.
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Real World Evidence Manager VrtxBoston, MA $132k–$132k12d Design and execute epidemiologic observational research to assess natural history and real-world outcomes for Vertex's pipeline and portfolio products.
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