Biostatistics and Safety
650 open positions
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Associate Director, Real World Biostatistics GskUSA - Pennsylvania - Upper Providence 1mo 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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VP, Biometrics AbCelleraRemote 1mo 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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Associate I, Clinical Pharmacology Scientific Support & Reporting AbbVieNorth Chicago, IL, us 1mo Prepare scientific reports, presentations, and Phase 1 protocols for clinical trials while assisting with blinded efficacy and safety reviews.
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Senior Director, Statistical Innovation↗ IpsenLondon, England, UK 1mo Leads innovative methodology, advanced modelling, and data-driven decision support across Ipsen's R&D portfolio to strengthen development strategy through design, simulation, and predictive analytics.
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Senior Statistical Programmer – CDISC Lead MyhrabcWEMEA > Spain > Remote 1mo 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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Associate Principal Scientist, Statistical Programming MsdRemote $145k1mo 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 Clinical Statistical Programmer (Portfolio Development / Biometrics / Programming) CslEMEA, GB, Berkshire, Maidenhead, CSL Behring 1mo 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 Statistician II AstraZenecaUS - Durham - NC $120k1mo 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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Associate Director / Director, Biostatistics↗ Novartis IrelandDublin, County Dublin, Ireland €104k–€193k1mo Provide strategic statistical leadership for Health Technology Assessment (HTA), pricing, reimbursement, and market access activities to support access to innovative medicines.
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Biostatistician (Neurology) JhuRemote $57k1mo 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 $156k1mo 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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Associate Director / Director, Biostatistics↗ Novartis UKLondon, England, UK £84k–£155k1mo Provide strategic statistical leadership for Health Technology Assessment (HTA), pricing, reimbursement, and market access activities to support access to innovative medicines.
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Director, Scientific Sales & Delivery↗ Pharmo Institute, Part of LumanityLondon, England, UK 1mo Strategic interface between clients and research team, combining epidemiological expertise with business development to lead RWE projects from qualification to completion.
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Stability Manager VaxcyteSan Carlos, California $147k1mo Manage cGMP stability programs for preclinical and clinical vaccine development projects, ensuring data integrity and regulatory compliance.
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Associate Director-Biostatistics↗ Rti Health SolutionsRemote 1mo Lead statistical analysis planning and execution for clinical trials and real-world data, with a strong focus on patient-reported outcomes and clinical outcome assessments.
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Associate Director-Biostatistics↗ Rti InternationalRemote 1mo Lead statistical analysis planning and execution for clinical trials and real-world data, with a strong focus on patient-reported outcomes and clinical outcome assessments.
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Director Respiratory Bioequivalence Strategy Lead ViatrisSandwich, England, United Kingdom 1mo Leads bioequivalence strategy for respiratory product development programs to ensure regulatory compliance and optimize in-vivo performance.
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Staff GMP Statistician RegeneronRENSS - GLOBAL VIEW, US $103k1mo 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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Senior Statistical Programmer-Philippines InderoRemote 1mo 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 $112k1mo Apply statistical techniques to design, analyze, and report on clinical studies for solid organ transplantation diagnostics products.
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Director, CMC Quantitative Sciences ModernaTXNorwood, Massachusetts 1mo Lead a team of statisticians and data scientists to deliver advanced quantitative solutions for Chemistry, Manufacturing, and Controls (CMC) across the product lifecycle, including regulatory filings, lifecycle management, and automated monitoring of…
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Sr Programmer Analyst (SAS and Clinical Data Experience Required) ThermofisherTaguig City, Philippines 1mo Lead programmer for moderately complex clinical trials studies, performing advanced bioinformatics programming, data management, and validation using SAS.
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Senior RWE Biostatistician↗ FortreaEstonia 1mo Lead design, analysis, and interpretation of non-interventional and Real-World Evidence (RWE) studies for global pharmaceutical and biotechnology clients.
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Senior Statistical Analyst↗ ICON PlcReading, England, UK 1mo Senior Statistical Analyst leading observational research studies, real-world data analyses, and health outcomes research to support healthcare decision-making.
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Senior ADS Programmer↗ RocheWelwyn, England, UK 1mo Transform statistical analysis plans into high-quality, traceable programming deliverables (tables, listings, figures, dashboards) for clinical studies, ensuring compliance with regulatory standards and generating data insights.
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Senior Statistical Programmer-Argentina↗ Indero (formerly Innovaderm)Remote 1mo Lead statistical programming for clinical trials, developing and validating annotated Case Report Forms (aCRFs), SDTM/ADaM datasets, and TLFs for regulatory submissions and interim analyses.
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Real World Evidence Manager VrtxBoston, MA $132k1mo 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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Senior Statistical Programmer (Permanent role) ClinChoiceRemote 2mo Lead statistical programming activities for clinical trials, delivering derived datasets, tables, figures, and listings for pharmaceutical and biotech clients.
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2027 Summer Intern Opportunities, Morristown, NJ SanofiMorristown, NJ $67k2mo Summer internship/co-op in Market Access, Quantitative Pharmacology (PKDM), or Drug Product Development within a biopharma company.
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Biostatistiker (m/w/d) Nuvisan ICB GmbHNeu-Ulm, BAYERN 2mo Planning, execution, and documentation of statistical analyses for Phase I-II clinical trials, including sample size calculation, randomization, and report creation.
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SAS Programmer - Advanced Degrees MedpaceCincinnati, Ohio 2mo Write SAS programs to create analysis datasets, tables, listings, and figures for clinical development services.
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