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Data & AI
› Biostatistics and Safety
Biostatistics and Safety
648 open positions
Biostatistics Manager
Amgen
Taiwan - Taipei
1mo
Provide statistical expertise, author/review study documents, and perform data analyses for clinical studies across the drug development lifecycle.
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Biostatistical Programming Senior Associate
Amgen
Taiwan - Taipei
1mo
Perform hands-on statistical programming to support complex data analysis of clinical studies and regulatory submissions.
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Associate Director, Biostatistics
Bms
Remote - United States - US
$190k–$230k
1mo
Lead biostatistician guiding the design, execution, and interpretation of statistical analyses for clinical oncology trials to develop radiopharmaceutical therapies.
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Alnylam Pharmaceuticals – Regulatory Affairs Postdoctoral Research Fellow
Northeastern
Boston, MA (Main Campus), US
$60k
1mo
Two-year postdoctoral fellowship supporting global regulatory strategy and drug development for RNAi therapeutics.
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Senior Biometrics Transformation Lead - M/W (CDI)
Pierrefabre
Haute Garonne (31), FR
1mo
Lead the transformation of the biometrics operating model for clinical development, statistics, and statistical programming to improve delivery predictability, quality, and governance.
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Director, Statistical Programming, Pharmacometrics
Regeneron
TARRYTOWN, US
$205k
1mo
Lead strategic programming initiatives and pharmacometric analyses to support clinical development programs from studies through regulatory submissions.
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Associate Director, Biostatistics
Bristolmyerssquibb
Remote
$190k
1mo
Lead biostatistician guiding design, execution, and interpretation of statistical analyses for clinical oncology trials to develop radiopharmaceutical therapies.
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Vertex – Early Development Postdoctoral Research Fellow
Northeastern
Boston, MA (Main Campus), US
$60k
1mo
Two-year postdoctoral fellowship for Pharm.D. graduates to advance clinical pharmacology, modeling & simulation, and early development medical strategies in drug development.
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Evidence Manager
Novartis
Taipei, TW
1mo
Lead the adaptation of global evidence strategies to the Taiwan market, translating them into actionable local plans and driving real-world evidence activities to support healthcare decision-making.
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Junior Statistical Programmer Analyst _Permanent Role_(CANADA)
ClinChoice
Remote
1mo
Junior Statistical Programmer supporting clinical trial programming activities, dataset development, and regulatory submissions for pharmaceutical and biotechnology clients.
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Senior Manager, Statistics
AbbVie
North Chicago, IL, us
1mo
Provide statistical leadership for clinical trials, patient safety, and global medical affairs to advance oncology medicines.
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Intern, Infectious Disease Epidemiology
ModernaTX
Cambridge, Massachusetts, US
1mo
Full-time summer intern supporting clinical trial conduct and post-marketing observational research for Moderna's infectious respiratory and gastrointestinal virus vaccine portfolio.
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Senior/Principal Statistician
Veramed
Remote
1mo
Provide high-quality statistical support, oversight, and project leadership for clinical studies and regulatory submissions.
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Statistical Science Director - Oncology
AstraZeneca
UK - Cambridge
1mo
Lead a biometrics team to deliver statistical design, delivery, and interpretation for pharmaceutical product development and regulatory submissions.
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Associate Director, Biostatistics
Bms
Uxbridge - GB
1mo
Design clinical trials, develop analysis plans, interpret results, and prepare regulatory submissions for drug development assets.
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Statistical Science Director - Oncology
AstraZeneca
Cambridge, , United Kingdom
1mo
Lead a biometrics team to deliver statistical design, delivery, and interpretation for oncology product development, regulatory submissions, and health technology assessments.
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Associate Director, Biostatistics
Gilead
United States - California - Foster City
$196k
1mo
Provide strategic and operational statistical leadership for clinical development programs in the Virology Therapeutic Area, ensuring high-quality statistical planning, analysis, and reporting for Phase 1–3 trials.
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Group Leader – Study Support Specialist (GLP studies – Product Safety Labs)
Eurofins
Bengaluru, KA, in
1mo
Lead a team of support staff to manage GLP-compliant preclinical safety studies, ensuring data quality, regulatory compliance, and on-time delivery for toxicology and product safety labs.
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SAS Programmer (Navi Mumbai)
Medpace
Navi Mumbai, India
1mo
Write SAS programs to create analysis datasets, tables, listings, and figures for clinical development projects.
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Experienced SAS Programmer (Navi Mumbai)
Medpace
Navi Mumbai, India
1mo
Senior SAS Programmer leading biostatistics projects to create analysis datasets, tables, listings, and figures for clinical trials.
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Centralized Statistical Monitoring, Senior Manager
Amgen
United States - Remote
1mo
Provide statistical, technical, operational, and business leadership for Centralized Statistical Monitoring (CSM) to ensure study quality oversight is scientifically rigorous, scalable, and inspection-ready.
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Associate Director I/II, Real World Data Statistics
AstraZeneca
Bangalore, , India
1mo
Lead the development of regulatory-grade evidence from real-world data (disease registries, patient cohorts) to support rare disease therapies and regulatory submissions.
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Senior Scientist, Quantitative Modeling & PK
Csl
EMEA, CH, Glattbrugg, CSL Behring
1mo
Apply quantitative modeling and pharmacokinetics to support non-clinical drug development, from candidate selection to first-in-human dose prediction.
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Associate Director I/II, Real World Data Statistics
AstraZeneca
India - Bangalore
1mo
Lead the development of regulatory-grade evidence from disease registries and longitudinal observational cohorts to support rare disease therapies and regulatory submissions.
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Sr Programmer Analyst
Thermofisher
Remote, Mexico
1mo
Lead programmer for moderately complex clinical trials studies, developing and validating statistical programs to manage data across multiple systems and generate reports/tables/figures.
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Biostatistiker*in (w/m/d)
Universitätsmedizin Göttingen
Göttingen, NIEDERSACHSEN
1mo
Biostatistician providing statistical support for clinical studies and research projects in medicine and genomics.
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Statistical Programmer I
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Everest Clinical Research
Remote
$45k–$55k
1mo
Develop and validate SDTM and ADaM datasets, SAS programs for statistical output, and data listings/tables to support clinical trial analysis and regulatory reporting.
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Medical Affairs Team Lead - Clinical Evidence and Statistics
Ogt
Cambridge, UK
1mo
Leading the Clinical Evidence and Statistics function to oversee clinical evidence generation, study design, statistical operations, and data analysis for genomic product development and regulatory submissions.
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Senior Statistical Programmer
Sanofi
Hyderabad, IN
1mo
Implement statistical analysis plans and provide QC'd data packages (tables, figures, listings) for publications and ad-hoc analysis requests.
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Principal Biostatistician (VAX)
Sanofi
Hyderabad, IN
1mo
Lead end-to-end biostatistics and programming activities for clinical studies in the Vaccines R&D value chain, from design to submission.
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Scientific Director, Clinical Pathology
Bristolmyerssquibb
New Brunswick - NJ - US
$239k
1mo
Provides expert scientific interpretation and integration of clinical pathology data from nonclinical development studies to support safety assessment and regulatory submissions.
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Real World Evidence Strategy Lead
Sanofi
Morristown, NJ, US
1mo
Establish and execute Real-World Evidence (RWE) strategies to translate medical needs into evidence driving regulatory, access, and medical decisions for global therapeutic areas.
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Senior Statistical Programmer
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Everest Clinical Research
Remote
$90k–$140k
1mo
Lead statistical programming for clinical trial data to support regulatory submissions and ensure data quality for pharmaceutical and biotech clients.
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Senior Biostatistician
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Parexel
Uxbridge, England, UK
1mo
Lead research design and analytical strategies for clinical trials, developing statistical analysis plans and authoring reports/manuscripts to support new therapies.
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Associate Director Quantitative Pharmacology
Regeneron
Remote
$176k
1mo
Lead model-informed drug development strategies to inform dose selection, trial design, and regulatory strategy for therapeutic areas including antibodies, siRNA, and gene therapies.
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Senior Biostatistician FSP
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Cytel
1mo
Senior Biostatistician supporting Phase I-IV clinical studies and regulatory submissions for pharmaceutical clients.
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Biostatistician - F/M/X
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Amaris Consulting | Part of Mantu
1mo
Analyze clinical and observational study data to support statistical interpretation and decision-making in Life Sciences projects.
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Senior Statistical Programmer - FSP
Iqvia
Nairobi, Kenya
1mo
Design, develop, and quality control SAS programs to access, extract, transform, review, analyze, and submit clinical data for regulatory submissions.
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Senior Manager, Statistics
AbbVie
North Chicago, IL, us
1mo
Provide statistical leadership for clinical trials, patient safety, and global medical affairs to advance medicines to patients.
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Senior Scientist, Toxicology I
AbbVie
North Chicago, IL, us
1mo
Function as GLP Study Director for internal toxicology studies and external sponsor monitor for CRO-conducted studies, ensuring regulatory compliance and report authorship for drug submissions.
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Pharmacokineticist, PPK/PD
Regeneron
TARRYTOWN, US
$110k
1mo
Senior independent contributor leading end-to-end non-compartmental and compartmental PK/PD analyses for nonclinical and clinical studies, preparing regulatory datasets, and supporting CRO studies.
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Senior Biostatistician II
Vrtx
Boston, MA, US
$132k
1mo
Designs, develops, and executes statistical infrastructure for clinical trials, observational studies, and real-world data investigations in drug development.
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Vice President, Biostatistics
4dmoleculartherapeutics
Remote
$330k
1mo
Enterprise-level strategic statistical leadership and oversight for global drug development programs, driving quantitative decision-making and regulatory strategy.
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Executive Director, Statistical Programming
4dmoleculartherapeutics
4D Molecular Therapeutics HQ
$298k
1mo
Provide strategic and operational leadership for statistical programming across clinical development programs, ensuring rigorous quality review of deliverables and establishing scalable standards.
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Senior Statistical Advisor-Canada
Indero
Montreal, Canada
1mo
Provide statistical input into Phase I-IV clinical trial development, assist in protocol development, support data analysis, and advise on trial design for a dermatology CRO.
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R&D and Regulatory Systems Lead
Viatris
Remote
$95k
1mo
Lead technical design, development, and integration of Veeva RIM Vault solutions to support global R&D and regulatory compliance processes.
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Associate Director, Biostatistics
Alnylam Pharmaceuticals
United States
$185k
1mo
Lead statistical activities for clinical trials, including design, protocol writing, analysis planning, and data interpretation for drug candidates.
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Principal Scientist, PSSM ARD, GMP Analytics, Stability Strategy & Operations
Pfizer
United States - Connecticut - Groton
$106k
1mo
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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Associate Director, Real World Biostatistics
Gsk
USA - 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
AbCellera
Remote
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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