Biostatistics and Safety
415 open positions
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Clinical Data Science Programmer IconIndia, Chennai 29d Develop and validate statistical programming code to support data analysis and reporting for clinical trials.
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CMC Statistics Director VrtxBoston, MA $193k–$193k29d Strategic and technical leadership for statistical sciences across the pharmaceutical product lifecycle, including process development, manufacturing, validation, and regulatory submissions.
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Principal Statistician - Permanent Role -Remote in UK ClinChoiceRemote 29d 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-UniversityBoston, MA, us 29d 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 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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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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Statistical Programming, Associate Director AstraZenecaIndia - Bangalore 1mo Lead statistical programming activities for clinical study planning, execution, and delivery, including clinical study report development and regulatory submissions for oncology products.
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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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Senior Pharmacometrician AbbVieNorth Chicago, IL, us 1mo 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, Quantitative Systems Pharmacology AlnylamUnited States 1mo Lead QSP modeling and simulation to support RNAi therapeutic drug development, focusing on dose selection, trial design, and mechanistic understanding of disease-treatment interactions.
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Associate Principal Scientist, Statistical Programming MsdUSA - New Jersey - Rahway $145k–$145k1mo Develop statistical programming analysis and reporting deliverables for global stakeholders in clinical trials, transforming data into analysis datasets and creating tables/figures per analysis plans.
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Principal Global SLC Pre-Sales Consultant – Healthcare and Life Sciences MendixLondon 1mo Technical consultant supporting account executives in the sales process for SAS Language Compiler (SLC), focusing on feasibility, porting, and modernization of SAS code for the pharmaceutical industry.
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Principal Biostatistician (FTE or Contract) EclinicalsolutionsRemote $175k–$175k1mo Lead statistical analysis, reporting, and programming for clinical trials, serving life sciences clients to accelerate clinical development.
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Senior Principal DSX Data Scientist, AI RocheSouth San Francisco $207k–$207k1mo Design and evolve next-generation statistical computing platforms, automate programming workflows, and create reusable coding macros to streamline evidence generation in clinical development.
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Senior Principal Statistician, Biometrics FerringParsippany, New Jersey, United States $191k–$191k1mo Design, execute, analyze, and report on clinical development programs and real-world evidence (RWE) studies to inform regulatory and business decisions.
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Programmer Analyst II (SAS and Clinical Data Experience Required) ThermofisherTaguig City, Philippines 1mo 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 BioSciencesParsippany, New Jersey $141k–$141k1mo 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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Principal Statistician - Point of Care (Ottawa)↗ AbbottOttawa, ON, CA $100k–$100k1mo Design, analyze, and interpret statistical results for clinical protocols and reports to support medical device regulatory submissions and transform health management decision-making.
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Sr. Scientist II - Toxicology - Onsite in Aliso Viejo, CA↗ GlaukosAliso Viejo, CA, US 1mo Leading and executing nonclinical toxicology programs for novel drug delivery devices and combination products to support clinical development and regulatory submissions.
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Clinical Business Development Associate (Remote Based / Sales Support) PciservicesRemote $51k–$51k1mo Supports Business Development Executives by creating clinical packaging and distribution proposals, calculating complex costs, and managing proposal revisions for biopharma clients.
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Senior Biostatistician↗ Srm TechnologiesTN, IN 1mo Provides statistical expertise for clinical trial design, analysis, and reporting, ensuring scientifically sound and regulatory-compliant statistical methodologies.
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(Senior) Principal Statistical Programmer↗ Beone MedicinesRemote, US $144k–$144k1mo Lead statistical programming for multiple clinical studies, producing analysis datasets, tables, listings, and graphs for regulatory submissions and publications.
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Director, Epidemiology & HEOR Consulting↗ NorstellaRemote 1mo Lead design and execution of real-world evidence, epidemiology, and health economics and outcomes research (HEOR) engagements for life sciences clients, serving as a senior scientific and strategic advisor.
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Senior Analyst I - Trial Analytics, Insights & Planning (TAIP)↗ Bristol Myers SquibbHyderabad, Telangana, India 1mo Senior Analyst supporting drug development through trial forecasting, feasibility analysis, and protocol planning within an internal consulting model.
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Principal Statistical Programmer - SDTM team↗ Cytel 1mo Lead statistical programming for clinical trials, developing automated reports and submission data packages for pharmaceutical and biotech clients.
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Associate Director, Statistical Programmer↗ Merck KgaaTS, IN 1mo Lead statistical programming activities to turn complex clinical trial data into high-quality deliverables for regulatory submissions and analysis.
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Clinical Data Scientist / Biostatistician↗ CapgeminiBarcelona, CT, ES 1mo Support and improve clinical algorithms for kidney disease, perform statistical analysis on real-world health data, and contribute to regulatory submissions for European market products.
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Senior Manager, Statistical Programming↗ Kite PharmaRemote, US $154k–$154k1mo Lead statistical programming for clinical trial analysis datasets and regulatory reports for cancer immunotherapy products.
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Manager Statistical Programming RegeneronWarren, US $129k–$129k1mo Lead statistical programming deliverables for clinical studies from development through regulatory approval and product launch.
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Senior Director, Real World Evidence Generation↗ DompéSan Mateo, CA, US $285k–$285k1mo Leads strategic design and execution of real-world data and evidence generation initiatives to support clinical value, market access, and lifecycle management goals.
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Senior Manager, Biostatistics EikontherapeuticsJersey City, New Jersey $170k–$170k1mo Lead statistical efforts for clinical trial design, execution, and analysis to guide R&D initiatives in biopharmaceutical drug discovery.
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Director, Nonclinical Development OrganonUSA - New Jersey - Florham Park $152k–$152k1mo Provide nonclinical subject matter expertise and serve as the nonclinical representative on asset development teams to support life-cycle management of products in Organon's portfolio.
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