Biostatistics and Safety
397 open positions
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Principal Statistical Programmer FSP↗ Cytel IncIN 26d Lead statistical programming for clinical development programs, generating datasets, tables, and reports for regulatory submissions while overseeing CRO deliverables.
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Research Assistant/Associate (Statistics)↗ Cardiff UniversityCardiff, WLS, GB $34k–$34k26d Design, manage, analyze, publish, and disseminate research for clinical trials using statistical methods.
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Bioanalysis and Toxicokinetics Project Manager - Client-dedicated ThermofisherCambridge, United Kingdom 26d Provide flexible scientific and project-management support across Bioanalysis, Toxicokinetics, and cross-functional operational improvement activities for drug discovery and development.
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Regulatory Submissions Specialist AbCelleraVancouver $93k–$93k27d Spearhead electronic publishing of clinical development submissions to ensure compliance with regional regulatory authorities.
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SAS Programmer I Psi-CroBuenos Aires, Buenos Aires, ar 27d Develop analysis data sets, program requirements, and SAS code for ADS, Tables, Listings, and Figures to support global clinical trials.
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R&D Clinical PK & Pharmacometrics Sr. Scientist MsdJPN - Tokyo - Chiyoda 27d Leverage clinical pharmacology and pharmacometrics to support drug development strategy, ensure early approval, and provide clinical pharmacology/PK information to clinical teams.
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Clinical Biostatistician I↗ AbbottRemote $61k–$61k27d Develop and establish evidence for molecular tests in oncology for screening, diagnosis, prognosis, monitoring, and therapy selection.
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Sr. Lead Biostatistician - Oncology Evidence Generation LabcorpDurham NC, US 27d Statistical lead for oncology evidence generation, designing and analyzing observational clinical validity studies, registries, and real-world evidence programs for minimal residual disease (MRD).
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Manager - Exploratory Analysis (Hybrid) AbbVieNorth Chicago, IL, us 28d Statistical expert supporting drug discovery, target identification, and clinical biomarker exploration to characterize patient subgroups and disease progression for precision medicine.
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Senior Statistician - Permanent Role -Remote in UK ClinChoiceRemote 28d Design and analyze clinical trials for pharmaceutical, biotechnology, and medical device clients, ensuring statistical validity and regulatory compliance.
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Statistical Programmer II↗ Cognitive Research CorporationRemote, US 28d Create and validate statistical programs, datasets, and outputs (TLFs) by transforming raw clinical trial data into CDISC-compliant deliverables for regulatory submissions.
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Head of Benefit-Risk and Pharmacoepidemiology↗ SanofiCambridge, MA, US 28d Lead epidemiology and benefit-risk strategies for product development and marketed products to characterize risks and inform safety decisions for regulatory authorities and internal governance.
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Principal Statistical Programmer↗ NovartisTS, IN 28d Lead statistical programming and data review for Phase I-IV clinical studies, ensuring high-quality deliverables for regulatory submissions and safety reports.
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Manager, Companion Animals Global On-market Clinical Studies & Outcomes Research↗ ZoetisRemote, US $93k–$93k28d Plan and execute global clinical studies and outcomes research to demonstrate the technical, emotional, and economic value of Zoetis companion animal products.
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（Senior）Statistician AstraZenecaChina 28d Provide statistical consultancy and expert support for clinical study design, data analysis, and regulatory submissions in biostatistics.
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Biostatistical Programming Senior Associate↗ AmgenTS, IN 28d Perform hands-on statistical programming to support complex data analysis of clinical studies and regulatory submissions.
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Toxicology Scientist - Advanced ExxonMobilShanghai, CN 29d Predictive/computational toxicologist applying in silico methods, mechanistic toxicology, and data-driven approaches to support chemical risk assessment and regulatory decision making.
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Sr. Manager, Quality Assurance AlnylamRemote $227k–$227k29d Design and execute real-world data (RWD) analyses and build economic models to support value propositions for late-stage and marketed biopharmaceutical therapies, specifically in rare disease areas.
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Nonclinical Toxicology Study Monitoring Scientist VrtxBoston, MA $102k–$102k29d Provide scientific, technical, and operational oversight of outsourced nonclinical safety studies (toxicology) for small and large molecule modalities including cell and gene therapies.
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Associate Functional Programmer↗ Novo Nordisk, Inc.KA, IN 29d Develop monitoring reports and customize data programs to support Risk-Based Quality Management (RBQM) and ensure quality/safety of clinical trials.
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Manager, Biostatistics - Hematology RegeneronTARRYTOWN, US $129k–$129k29d Lead biostatistical strategy and analysis for clinical trials in hematology drug development.
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Associate Director, Biostatistics - IQVIA Biotech (m/w/d)↗ IqviaRemote 29d Lead Statistician providing senior-level statistical review, oversight, and leadership for clinical programs in oncology, CNS, immunology, and cardiovascular therapy areas.
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?Senior Principal Scientist (m/w/d) Ingelheim am Rhein, RHEINLAND_PFALZ 1mo Lead and execute clinical Quantitative Systems Pharmacology (QSP) modeling projects to drive model-informed decision making across drug development programs.
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Associate Director/Sr. Manager, Health Economics & Outcomes Research-Oncology NateraUS 1mo Lead the development and execution of health economic and outcomes evidence demonstrating the clinical and economic value of Natera's precision molecular diagnostic technologies across oncology.
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Clinical Data Science Programmer IconIndia, Chennai 1mo Develop and validate statistical programming code to support data analysis and reporting for clinical trials.
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Associate Director of Statistical Programming Harvard-UniversityBoston, MA, us 1mo 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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Principal Global SLC Pre-Sales Consultant – Healthcare and Life Sciences Siemens-EdaVirtual, USA, United States $1062k–$2017k1mo Technical consultant supporting account executives in the sales process for SAS language modernization projects, specifically porting code to SLC (SAS Language Cloud) within the pharmaceutical industry.
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Staff Clinical Scientist WhoopBoston, MA $170k–$170k1mo Senior scientific leader shaping clinical evidence strategy and leading complex clinical programs for WHOOP's health and fitness wearable.
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Principal Statistician GskJapan - Tokyo - Akasaka 1mo Lead biostatistical activities for clinical research programmes to support drug and vaccine development for Japanese patients, ensuring regulatory compliance and optimizing trial designs.
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Clinical Data Scientist -RWE Data Analysis Oversight Lead: Inflammation GileadUnited States - New Jersey - Parsippany $206k–$206k1mo 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 Consultant (Life Sciences – Compliance) BakertillyUSA DC Washington DC $81k–$81k1mo Senior Consultant providing risk advisory, compliance, and ethics services to life sciences clients, focusing on regulatory compliance, reimbursement policies, and fair market value analysis.
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