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Data & AI
› Biostatistics and Safety
Biostatistics and Safety
656 open positions
Principal Programmer/Associate Manager - Statistical Programming, Central Services
Regeneron
Hyderabad
2mo
Lead statistical programming for integrated analysis, regulatory submissions, and clinical trial disclosure activities.
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Principal Statistician - Permanent Role -Remote in UK
ClinChoice
Remote
2mo
Lead statistical activities and strategy for clinical trials across pharmaceutical, biotechnology, medical device, and consumer health projects.
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Associate Director of Statistical Programming
Harvard-University
Boston, MA, us
2mo
Leading statistical programming efforts, infrastructure, and quality systems for NIH-funded clinical research networks (ACTG, IMPAACT) to support HIV and infectious disease treatment/prevention studies.
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Director, Clinical Programming
AstraZeneca
Spain - Barcelona
2mo
Senior leader responsible for shaping and delivering high-quality clinical programming, overseeing both outsourced and in-house activities to support evidence generation and the Statistics group.
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Senior Principal Biostatistician/Senior Manager, Biostatistician - Study Lead (Oncology) - Remote
ClinChoice
Remote
2mo
Lead statistical activities and strategy for clinical trials, primarily in Oncology, ensuring regulatory compliance and delivering high-quality analysis.
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Senior Director, RWE Lead in Inflammation Therapeutic Areas
Gilead
United States - California - Foster City
2mo
Lead the global Real-World Evidence (RWE) strategy for Inflammation products to support clinical development, regulatory submissions, and commercialization.
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Clinical Data Scientist -RWE Data Analysis Oversight Lead: Inflammation
Gilead
United States - New Jersey - Parsippany
$206k
2mo
Oversees timeliness and quality of Real-World Evidence (RWE) analysis results for the Inflammation therapeutic area, managing vendor performance and analysis workflows in a GxP compliant environment.
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Senior Pharmacometrician
AbbVie
North Chicago, IL, us
2mo
Conceive, execute, and communicate multi-disciplinary modeling and simulations to support drug development plans, commercial goals, and regulatory requirements; generate new PK/PD modeling proposals and optimize methods in statistical data analysis.
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Associate Director, Biostatistics
Bms
Princeton - NJ - US
$218k–$264k
2mo
Lead biostatistics for clinical trial design, analysis planning, and regulatory submissions across a specific indication or therapeutic area.
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Statistical Science Director
AstraZeneca
India - Bangalore
2mo
Lead statistical strategy and design for global medicine development, guiding programs from early discovery through registration to influence patient outcomes and business value.
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Senior Statistical Programmer
AstraZeneca
Spain - Barcelona
2mo
Lead statistical programming for clinical studies, transforming complex clinical data into decision-ready evidence for global regulatory submissions.
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Programmer Analyst II (SAS and Clinical Data Experience Required)
Thermofisher
Taguig City, Philippines
2mo
Perform bioinformatics programming and data analysis for clinical research projects, including data transfer, validation, and report generation.
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Associate Director, Late Phase Research Biostatistics
Pacira BioSciences
Parsippany, New Jersey
$141k
2mo
Lead statistician providing leadership and guidance for late-phase clinical studies, ensuring statistical validity and strategy for observational and investigational designs.
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Consultant, Advanced Analytics: Meta-Analysis (HTA Statistician)
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Parexel
Uxbridge, England, UK
2mo
Statistical and methodological leadership for clinical development programs, focusing on Access/HTA evidence generation, systematic reviews, and network meta-analysis to support global commercialization and reimbursement strategies.
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Principal Biostatistician
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Fortrea
Remote
2mo
Lead statistical strategy and delivery for complex clinical trials from study design through regulatory submissions.
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Principal Statistical Programmer - SDTM team
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Cytel
3mo
Lead statistical programming for clinical trials, developing automated reports and submission data packages for pharmaceutical and biotech clients.
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Manager, Statistical Programming - Starszy Programista
Bms
Warsaw-WeWork-PL
238k
3mo
Design, develop, and implement technical solutions for integrating, analyzing, and reporting clinical data to support regulatory approval and market acceptance of pharmaceutical products.
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Benefit-Risk Excellence Lead (Sr PV Manager) - client-dedicated for 12 months
Thermofisher
Remote, Serbia
3mo
Lead short- and mid-term projects to drive innovation and excellence in Benefit-Risk Assessment & Management (BRAMS), enhancing procedures and supporting digital transformation within signal detection and safety writing systems.
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Statistical Science Director
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AstraZeneca
Bengaluru, Karnataka, India
3mo
Lead statistical strategy and evidence generation for global medicine development from early discovery through registration, influencing decisions on therapeutic progression and investment.
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HTA & Modelling Science Lead
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AstraZeneca
Barcelona, Catalonia, Spain
3mo
Lead health economic modelling and budget impact analysis to develop evidence for HTA submissions and secure patient access to oncology medicines globally.
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[DJ] 非臨床開発研究部 [DSRD] リサーチアンドディベロップメントサイエンティスト(専門管理職・一般社員)/Research and Development Scientist (Research & Development Scientist / DSRD-Tokyo)
Pfizer
Japan - Tokyo
3mo
Lead non-clinical regulatory affairs and strategy for pharmaceutical approvals in Japan, managing toxicology, pharmacology, and pharmacokinetics data for regulatory submissions.
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Senior/Principal Clinical Pharmacologist
AstraZeneca
Shanghai Jing'An Office, CN
3mo
Lead clinical pharmacokinetics (PK), pharmacodynamics (PD), and modelling & simulation (M&S) to justify dosing strategies and support regulatory submissions for drug development programs.
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R Programmer
Medpace
London, United Kingdom
3mo
Develop and validate data products (primarily Shiny applications) to increase operational efficiency for clinical trials.
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Statistical Programming Associate Director
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AstraZeneca
Barcelona, Catalonia, Spain
3mo
Lead statistical programming aspects of clinical development programs, ensuring high-quality deliverables and compliance with industry standards.
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Senior Statistical Programmer
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Everest Clinical Research
Remote
3mo
Design and generate statistical analysis data models and SAS code for clinical trial data tabulation and validation.
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Principal Research Scientist II
AbbVie
North Chicago, IL, us
3mo
Provide technical leadership for the development, evaluation, and lifecycle management of medical devices and combination products.
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Principal Scientist, Safety
Neurocrine
US CA San Diego
$131k
3mo
Lead scientific and clinical expertise for clinical and post-market pharmacovigilance, including signal management, benefit-risk evaluations, and authoring periodic safety reports.
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Statistics & Analysis Manager
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Abbott
Witney, England, UK
3mo
Lead a team of statisticians and analysts to shape statistical strategy, allocate resources, and ensure high-quality analysis for product development, clinical evidence, and regulatory submissions in Diabetes Care.
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Scientist, Safety
Neurocrine
US CA San Diego
$90k
3mo
Supports safety surveillance and risk management for Neurocrine products throughout the product lifecycle, including signal detection, analysis, and regulatory reporting.
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Translational Medicine Scientist (Contractor), Shanghai/Beijing
Pfizer
China - Shanghai - STIT
3mo
Design, prioritize, and execute clinical translational studies using disease biology and clinical trial sample analyses to inform drug development decisions in precision medicine.
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Senior/Principal Scientist, Radiation Science and Theranostic
AstraZeneca
Shanghai Jing'An Office, CN
3mo
Primary subject matter expert for molecular imaging workflows across clinical trial portfolios, ensuring SPECT/PET image acquisition, data transfer, and radiopharmaceutical handling comply with GCP and radiation safety standards.
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Biostatistician
Geisinger
Remote
3mo
Design clinical research studies, develop analysis plans, and perform biostatistical analyses for healthcare research.
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Senior Manager, Ontology
Takeda
Boston, MA
$137k
3mo
Hands-on R&D BioPharm data curator responsible for harmonizing Research, Development, and Global Medical data into standardized, analysis-ready, FAIR-aligned datasets.
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Data Scientist
Lonza
NL - Geleen
€56k–€78k
3mo
Serves as the Site Data Administrator and leads data science capabilities for process data analytics (CPV) and process validation at a pharmaceutical manufacturing facility.
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Senior Manager Statistical Programming
Regeneron
Warren, US
$151k
3mo
Lead statistical programming across multiple clinical studies to ensure timely, high-quality regulatory submission deliverables from study through product launch.
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Vice President, Biometrics and Clinical Analytics
Aditum Bio
Cambridge, Massachusetts
3mo
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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Research Scientist II – Extractables & Leachables (E&L) Team Lead
Baxter
Braine-l'Alleud
3mo
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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Feasibility Informatics Analyst
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Medpace
London, England, UK
3mo
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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MSAT Data Expert (Biologics)
Takeda
2 Locations
$116k
3mo
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 BioSciences
Parsippany, New Jersey
$102k
3mo
Lead biostatistical activities to support clinical development and post-marketing efforts, ensuring high-quality analytical outputs for regulatory decision-making.
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Biostatistician II
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Parexel
Uxbridge, England, UK
3mo
Lead statistical aspects for low to moderate complexity clinical studies, developing analysis strategies and executing them to support regulatory submissions and development decisions.
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Senior Principal Pharmacovigilance Scientist
Takeda
USA - MA - Cambridge - Kendall Square - 500
$137k
3mo
Ensures regulatory compliance and safety of Takeda's products by managing large pharmacovigilance projects, developing innovative solutions, and leading teams.
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Associate Director Statistical Programming
Regeneron
Warren
$176k
3mo
Oversee statistical programming activities across internal teams and functional service providers to ensure high-quality deliverables for therapeutic area programs.
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Biostatistical Analyst II (Remote Capable)
Geisinger
Remote
3mo
Provide biostatistical support for clinical research studies, from design and analysis plan development to data interpretation and publication support.
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2027 Spring Co-Op Opportunities, Morristown, NJ
Sanofi
Morristown, NJ
$56k
3mo
6-month co-op roles in Supply Chain Planning, Quantitative Pharmacology, or Digital Transformation within a biopharma R&D environment.
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Principal Scientist, Translational Modeling & Decision Science
Flagshippioneeringinc
Pioneering Intelligence
4mo
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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Director, Head of Predictive Modelling & Biopharmaceutics
Takeda
Boston, MA
$177k
4mo
Provides strategic and operational leadership for the Predictive Modelling and Biopharmaceutics function within oral drug product development, ensuring capabilities align with portfolio objectives.
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Principal ADS Program Lead
Roche
Boston, US
$136k
4mo
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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Associate Director of Data and Knowledge Management
Vaxcyte
Remote
$183k
4mo
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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Director Programming
Thermofisher
Bengaluru, India
4mo
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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