Biostatistics and Safety
396 open positions
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Director, Biostatistics Project Lead SanofiWaltham, MA $179k–$179k2mo Lead biostatistician providing scientific leadership and statistical oversight for large, business-critical vaccine projects in clinical development or post-marketing stages.
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Principal Consultant - Toxicology SoterahealthNelson Labs SLC, US 2mo Senior toxicology expert providing scientific direction for written assessments, risk evaluations, and regulatory responses for medical devices and pharmaceuticals.
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Associate Director, Biostatistics 4dmoleculartherapeuticsRemote $193k–$193k2mo Provide strategic statistical input and technical expertise to lead clinical trial projects for late-stage biotechnology programs, specifically in ophthalmology and gene therapy.
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Vice President, Biometrics and Clinical Analytics Aditum BioCambridge, Massachusetts 2mo Lead biometrics and clinical analytics for early-stage drug development, designing rigorous studies and delivering near-real-time visibility into clinical data.
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Feasibility Informatics Analyst↗ MedpaceLondon, England, UK 2mo Architect, mine, analyse, and visualise clinical trial data to inform study design choices and support proposal feasibility strategies for pharmaceutical development.
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Research Scientist II – Extractables & Leachables (E&L) Team Lead BaxterBraine-l'Alleud 2mo Lead a team of E&L Study Directors and drive strategic E&L programs for medical devices, pharmaceuticals, and combination products to support regulatory submissions and product lifecycle management.
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MSAT Data Expert (Biologics) Takeda2 Locations $116k–$116k2mo Design, implement, and maintain CMC data standards, taxonomies, and ontologies for biologics to ensure high-quality, analysis-ready data for MSAT and manufacturing use cases.
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Manager, Biostatistics Pacira BioSciencesParsippany, New Jersey $102k–$102k2mo Lead biostatistical activities to support clinical development and post-marketing efforts, ensuring high-quality analytical outputs for regulatory decision-making.
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Director, CPMS Oncology GskRemote $188k–$188k2mo Lead quantitative clinical pharmacology and modelling & simulation (CPMS) strategies for oncology drug development programs to inform dose selection, trial design, and regulatory submissions.
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Associate Director Statistical Programming RegeneronWarren $176k–$176k2mo Oversee statistical programming activities across internal teams and functional service providers to ensure high-quality deliverables for therapeutic area programs.
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System Design Analyst II - HYBRID AbbVieFlorham Park, NJ, us 2mo Design and develop clinical trial systems ensuring compliance with data standards, protocols, and regulations to support clinical data strategy.
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Senior Manager, Real-World Evidence (RWE) Biostatistician BristolmyerssquibbUxbridge - GB 2mo Curation, transformation, and analysis of complex healthcare datasets to inform evidence generation and support clinical program design and trial execution.
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Statistical Advisor GileadUnited States - California - Foster City $226k–$226k2mo Senior statistical expert advising study leads on complex trial designs, simulation, and adaptive software tools for clinical trials.
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Biostatistical Analyst II (Remote Capable) GeisingerRemote 2mo Provide biostatistical support for clinical research studies, from design and analysis plan development to data interpretation and publication support.
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Principal Scientist, Translational Modeling & Decision Science FlagshippioneeringincPioneering Intelligence 2mo A Principal Scientist who uses mechanistic modeling and quantitative analysis to reduce scientific uncertainty in drug development and investment decisions, bridging the gap between AI capabilities and real-world impact across a therapeutic portfolio.
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Principal ADS Program Lead RocheBoston, US $136k–$136k2mo Senior leader guiding technical strategy and operational execution for analytical data science across multiple clinical programs or therapeutic areas in pharmaceutical R&D.
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Health Technology Assessment Consultant with German - Working from Spain (hybrid or home-based) IqviaBarcelona, Spain 2mo Develop German AMNOG dossiers and perform scientific assessments of clinical trial data to support reimbursement and market access decisions for life sciences clients.
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Associate Director of Data and Knowledge Management VaxcyteRemote $183k–$183k2mo Lead enterprise-wide data governance, knowledge management, and digital transformation to ensure data integrity and regulatory readiness for vaccine development and clinical operations.
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Assoc Prin. Scientist I/II, Epidemiology MsdCHN - Beijing - Beijing (Wangjing Park) 2mo Design, conduct, and analyze pharmacoepidemiologic research studies for product safety risk management and post-marketing studies across Vaccine, Oncology, and General Medicine therapy areas.
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Director Programming ThermofisherBengaluru, India 2mo Provides operational leadership for the bioinformatics programming function, overseeing staff, resources, and technology to ensure efficient production of quality work for clinical trial projects.
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Scientist - Cardiovascular Safety Pharmacology LabcorpHuntingdon United Kingdom 2mo Collecting, analyzing, and validating cardiovascular safety data (ECG, blood pressure, respiratory waveforms) for drug development studies.
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Associate Director Senior Patient Safety Scientist AstraZenecaRemote 2mo Required skills: MD, MSc, PhD, or PharmD in a scientific field; Minimum of 6+ years of relevant experience; Patient Safety and/or Clinical/Drug Development proven experience working in safety and/or scientific activities in at least 3 of the following areas…
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[R&D] Statistician, バイオメトリクス・データマネジメント統括部 統計担当者 PfizerJapan - Tokyo 3mo Design, analyze, and interpret clinical trials and post-marketing surveillance (PMS) to support drug development and regulatory submissions.
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Principal / Associate Director, Statistical Programming MadrigalpharmaPA - Conshohocken - Office $180k–$180k3mo Lead and support statistical programming activities across multiple clinical studies to ensure high-quality data analysis and regulatory submissions for MASH therapeutics.
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Senior Risk Management Engineer / Scientist ViatrisNorthern Cross, Dublin, Ireland 3mo Establish, maintain, and remediate risk management files for medical devices and combination products throughout the product lifecycle, ensuring compliance with global regulations and standards.
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Translational Research Scientist IntuitiveRemote 3mo Lead translational research to understand mechanisms of action for medical interventions, translating biological and engineering insights into device design and clinical study plans for Class II and III pulmonary medical devices.
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Senior Director Biostatistics Head of Statistical Innovation & Methodology AlnylamRemote $247k–$247k3mo Provide scientific leadership in advanced statistical methodology, innovative trial design, and simulation-based approaches to address complex design and analysis challenges across clinical development.
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Director/Senior Director, Pharmacovigilance and Drug Safety (Safety Scientist) XenonBoston 3mo Lead proactive signal detection, benefit-risk analyses, and safety monitoring/reporting for clinical and marketed products across the full product lifecycle.
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