Biostatistics Jobs

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Data Scientist IV, Biostatistics

Kaiser Permanente

Oakland, California, USA

Full-time

Overview: Kaiser Permanente's Northern California (NCAL) Regional Pharmacy Operations is seeking a Data Scientist IV, Biostatistics to support a diverse range of pharmacy service domains, including ambulatory care, inpatient, outpatient, oncology, and supply chain. This role leverages Kaiser Permanente's broad longitudinal data to drive meaningful improvements in service delivery and patient outcomes. You will partner with various teams to assess populations and outcomes, evaluate workflows, e

Sr. Principal Statistics

PARAKEET WORLD SOLUTIONS LLC

Remote

Contract

Job Title: Sr. Principal StatisticsLocation: Remote Duration: 6 MonthsEmployment Type: W2 ContractExperience Level: Mid-SeniorEducation Required: Ph.D. or MS in Statistics or BiostatisticsIndustry: Pharmaceuticals Job Summary:The Sr. Principal Statistician will lead statistical activities in clinical trials, from protocol development to final study reporting. The role will also contribute to regulatory filings, in-licensing evaluations, and marketing support. Key Responsibilities:Review protocol

Director, Biostatistics

Proclinical Staffing

Washington Grove, Maryland, USA

Full-time

Job Description Director, Biostatistics - Permanent - Maryland, US Ready to shape the future of clinical statistics? Step into a pivotal leadership role as Director of Biostatistics with one of our forward-thinking clients. Primary Responsibilities: In this role, you will drive statistical strategies and technical activities, contributing to the development of life-changing medicines. This position offers the opportunity to collaborate across functions, mentor team members, and influence decisi

SAS Programmer III

Katalyst Healthcares and Lifesciences

Fremont, California, USA

Full-time

Responsibilities: 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, SOIs, and guidance documents. Create and maintain specifications as per SDTM/ADaM standard and study SAP. Define and create ad-hoc reports and listings for clinical teams. Develop, implement and maintain SAS programming standards. Builds/tests programs for Data Validation, Derivation, and

Data Scientist III

University of Pittsburgh

Pittsburgh, Pennsylvania, USA

Full-time

Job Summary Job Title: Data Scientist Job Location: Pittsburgh, PA Job Description Contribute to develop data analysis plans. Statistical programming using statistical software for data analysis. Communicate analytical findings to diverse audiences including Principal Investigators, research partners and colleagues. Independently work on projects with minimal input from PI. Lead development, dissemination, and implementation of reproducible statistical programs for a multi-state, multi-year

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

South San Francisco, California, USA

Full-time

Responsibilities: Performs all SAS programming required for clinical trial analysis and reporting. Ensures that activities and processes performed are conducted according to sponsor requirements. Works closely with the Biostatistics and Data Management departments on various clinical projects. Designs and/or reviews database structure. Writes edit checks from the Data Cleaning Plan (DCP) specifications. Creates derived-analysis datasets. Executes analyses specified in the Statistical Anal

Senior Data Analyst

Zachary Piper Solutions, LLC

Remote

Full-time

Piper Companies is seeking a Senior Data Analyst to join a global leader in clinical research and healthcare analysis for a remote position . The Senior Data Analyst w ill lead statistical programming and analysis for oncology observational studies, managing complex datasets, ensuring quality control, and collaborating with scientists to drive meaningful insights from real-world evidence. Responsibilities of the Senior Data Analyst include: Lead statistical programming and analysis using oncolo

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Dallas, Texas, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Athens, Georgia, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

Princeton, New Jersey, USA

Full-time

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.

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Boulder, Colorado, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Lake Success, New York, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p

Experienced Data Scientist

Johnson & Johnson

Danvers, Massachusetts, USA

Full-time

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

SAS Programmer

Katalyst Healthcares and Lifesciences

San Diego, California, USA

Full-time

Responsibilities: Serves as lead programmer for assigned projects to provide statistical and programming support in one or more Phase I- clinical studies. Design and perform quality checks on analysis datasets, tables, listings, figures (TFL), and written reports to support clinical trial results using SAS. Create and review annotated CRF to STDM datasets. Produce and maintain technical programming specification documents. Lead and actively participate in client and project review meetings.

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

Edison, New Jersey, USA

Full-time

Responsibilities: Serve as the statistical programming lead on internal project teams and coordinate programming, verification, and documentation of statistical programs for use in creating analysis datasets, tables, listings, and figures. Facilitate advanced technical expertise, in conjunction with internal and external team members, to design, implement, validate, and maintain project reporting applications that are supported by the department. Assist in ensuring the optimum performance of

Clinical Safety Coder - MedDRA/WHODrug

General Dynamics Information Technology

Maryland, USA

Full-time

Type of Requisition: Regular Clearance Level Must Currently Possess: None Clearance Level Must Be Able to Obtain: None Public Trust/Other Required: NACI (T1) Job Family: Medical Affairs Job Qualifications: Skills: Clinical Research, MedDRA, WHODrugCertifications: NoneExperience: 6 + years of related experienceship Required: Yes Job Description: GDIT's Military Health team is hiring a Clinical Safety Coder - MedDRA/WHODrug to support the Office of Regulated Activities (ORA) under the DoD (D

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

San Diego, California, USA

Full-time

Responsibilities: Manage programming activities on project or study level, including managing CROs to ensure deliverables are accurate and compliant. Act as a Programming SME for assigned studies, including authoring/reviewing programming specifications, such as SDTM/ADaM specifications, TFLs creation and QC for reporting events, ESUB packages, and documenting production and validation programs. Apply programming skills to support statistical analysis, clinical reporting, regulatory submission

Senior SAS Programmer

Katalyst Healthcares and Lifesciences

Seattle, Washington, USA

Full-time

Responsibilities: The senior programmer position will be responsible for manipulating large databases and generating reports to enable analysts to explore real world healthcare data assets. Candidates must have excellent SAS and SQL programming skills and the ability to implement complex logic. Candidates must be comfortable with creating complex analysis data sets derived from various data sources with a careful eye for outliers and errors. Prior experience building patient cohorts and evalu

Senior Health Services Researcher

American Board of Internal Medicine

Philadelphia, Pennsylvania, USA

Full-time

Job DescriptionThe American Board of Internal Medicine (ABIM) is currently seeking a Senior Health Services Researcher to join our Assessment and Research team. The Senior Health Services Researcher will lead strategic research to evaluate Certification and Maintenance of Certification programs, design studies in health policy, physician performance, and product improvement. They will also collaborate with top research partners, mentor staff in advanced statistical methods, and oversees complex

Data Scientist II

Katalyst Healthcares and Lifesciences

Remote or New Jersey, USA

Full-time

Overview: The successful candidate will work with stakeholders in the Quantitative Medicine and Genomics (QM&G) organization to update and maintain existing data resources and visualization tools and develop new dashboard solutions for evaluating target predictions against observed data. Responsibilities: Update and maintain existing shiny app and Neo4J graph. Collaborate with team members to design and implement new framework solutions for data analysis and visualization. Develop dashboards