Biostatistics jobs

Statistical Project Leader, Biostatistics

Morristown, New Jersey

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Yesterday

Job Title: Statistical Project Leader, Biostatistics Location: Cambridge, MA Morristown, NJ About the Job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. As a Statistical Project Leader in Biostatistics, you will Lead one or more indications/projects in Oncology Development at Sanofi, under minimum supervision of seni

Full-time

Statistical Project Leader, Biostatistics

Cambridge, Massachusetts

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Today

Full-time

TA Head of Biostatistics, Neuroscience and Ophthalmology

Cambridge, Massachusetts

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Yesterday

Job Title: Data Governance Location: Cambridge, MA Morristown, NJ About the Job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. Join our Biostatistics Neuroscience and Ophthalmology teamas Global Head of Neuroscience and Ophthalmology TA Biostatistics. You will beleading and overseeing all statistical work for clinica

Full-time

TA Head of Biostatistics, Neuroscience and Ophthalmology

Morristown, New Jersey

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Today

Full-time

Biostatistician

Santa Clara, California

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12d ago

Infonex Technologies, Inc. has openings for a Biostatistician in Santa Clara, CA: Job Title: Biostatistician Job Duration: Full Time, Permanent, 40 Hours/Week Job Duties: Perform SAS/analytical programming, data management, quality control and reporting for research projects. Extract, manipulate, and merge large databases to create analytical datasets. Assist in defining analytical variables and consult with project staff on project needs. Maintain professional relationships with project personn

Easy Apply

Full-time

$152,610 - $165,000

Clinical SAS Programmer

Dallas, Texas

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Today

Responsibilities: Develop and maintain SAS programs to import, clean, and validate clinical trial data. Use R for data manipulation, analysis, and visualization. Perform statistical analyses in accordance with study protocols and analysis plans. Generate tables, listings, and figures (TLFs) using SAS and R. Create and QC statistical outputs and clinical study reports for regulatory submissions. Document programming activities and ensure compliance with Standard Operating Procedures (SOPs). Work

Full-time

Principal Biostatistician

King of Prussia, Pennsylvania

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Today

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Principal Biostatistician? The job is in our King of Prussia, PA, Waltham MA and Maidenhead UK office. This is a hybrid

Full-time

SAS Programmer- II

Atlanta, Georgia

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Today

Roles & Responsibilities: BS or above in computer science/statistics with at least 5 years of SAS experience in major pharma or CRO. Develop SAS coding for generating SDTM, ADaM datasets and TLFs to support clinical study analysis. Proficient computer skills across multiple applications and OS environments. Review and ensure accurate and high-quality statistical programming deliverables from CRO. Perform generation, validation and QC/QA of SDTM, ADam and TFL output in accordance with SOPs,

Full-time

Manager Research Integrity

Akron, Ohio

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Yesterday

Full-time, 40 Hours/Week Monday to Friday, 8am - 5pm Hybrid (Onsite 2-3 days/week) Summary: The Manager, Office of Research Integrity oversees the daily operations of the Office of Research Integrity, ensuring alignment with institutional goals and compliance with internal and external regulations. This role collaborates closely with Research Administration, Legal Services, and Compliance to support research integrity across the organization. The manager supervises staff and functions related t

Full-time

Manager Research Integrity

Doylestown, Ohio

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Yesterday

Full-time

Manager Research Integrity

Kent, Ohio

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Yesterday

Full-time

Manager Research Integrity

Cleveland, Ohio

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Today

Full-time

Manager Research Integrity

Brecksville, Ohio

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Today

Full-time

Clinical SAS Programmer

Omaha, Nebraska

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Today

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements Provides input in the design and development of case report forms and clinical databases Performs

Full-time

Clinical SAS Programmer

Boulder, Colorado

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Today

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases. Perfo

Full-time

Clinical SAS Programmer

Omaha, Nebraska

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Today

Full-time

Sr. SAS Programmer

Richmond, Virginia

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Today

Job Description: We are seeking a highly skilled Senior Statistical Programmer to join our growing Biometrics team. The ideal candidate will be responsible for providing advanced programming support for the analysis and reporting of clinical trial data in compliance with regulatory requirements. This role will involve working closely with Biostatisticians, Data Managers, and Clinical Teams to deliver high-quality datasets, tables, listings, and figures (TLFs). Responsibilities: Develop, validat

Full-time

Clinical SAS programmer

Tarrytown, New York

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Today

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures, and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases.

Full-time

Research Fellow-BST-AI and Informatics-Tao lab

Jacksonville, Florida

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Today

Job Description We are seeking a talented and motivated Healthcare AI and Data Analyst to join our department, focusing on the development and application of Natural Language Processing (NLP), Large Language Models (LLM), and deep learning techniques to address various clinical challenges. This role is pivotal in advancing our healthcare organization's capabilities in AI-driven research and clinical applications. The ideal candidate will have a strong background in AI, machine learning, and dat

Full-time

Statistical Programming Analyst II - CGS Administrators (Nashville)

Nashville, Tennessee

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Today

Summary Develops comprehensive reports and analyzes data in order to identify patterns and trends. Assists in creating materials that aid in illustrating analytical/data findings. Assists with sophisticated data interpretation, compilation, and verification to guide departmental efforts. Description Why should you join the BlueCross BlueShield of South Carolina family of companies? Other companies come and go, but we've been part of the national landscape for more than seven decades, with our r

Full-time

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Biostatistics jobs