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

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 with R Analytics Experience

Greymatter Innovationz

Pittsburgh, Pennsylvania, USA

Full-time

Job DescriptionGreymatter Innovationz helps you stay digitally relevant across domains, technologies, and skillsets, every day. We are looking for: Clinical SAS Programmer with R Analytics Experience Location: Pittsburgh, PA (Onsite/Hybrid preferred) Job Type: Contract / Full-Time Job Summary: We are looking for a Clinical SAS Programmer with strong experience in R-based analytics to support clinical trial data analysis and reporting. The ideal candidate will have expertise in statistical progra

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

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 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

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Boston, Massachusetts, 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. Perf

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

Research Data Scientist

Ascension Health

Remote

Full-time

Details Department: Ascension Data Science InstituteSchedule: Full timeLocation: RemoteBenefits Paid time off (PTO) Various health insurance options & wellness plans Retirement benefits including employer match plans Long-term & short-term disability Employee assistance programs (EAP) Parental leave & adoption assistance Tuition reimbursement Ways to give back to your community Benefit options and eligibility vary by position. Compensation varies based on factors including, but not limited to

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

Senior Clinical Data Analyst

Katalyst Healthcares and Lifesciences

Boston, Massachusetts, USA

Full-time

Job Description: This position focuses on assisting with analysing data and deriving insights from clinical and safety data sources to generate evidence and support decision making across the organization. The Associate will leverage a variety of analytics and visualization techniques to contribute to research, clinical development, drug safety and post-marketing activities. Responsibilities: Collaborates and works closely with cross-functional teams, including data analysts/engineers and busin

Cardiovascular Data Scientist

University Of Utah

Salt Lake City, Utah, USA

Full-time

Posting Details The University of Utah, an AA/EO employer, encourages applications from all qualified individuals, and provides reasonable accommodation to the known disabilities of applicants and employees. The University of Utah values candidates who have experience working in settings with students, staff, faculty and patients from all backgrounds and possess a strong commitment to improving access to higher education, employment opportunities, and quality healthcare for historically underre

Sr. SAS Programmer

Katalyst Healthcares and Lifesciences

Charlotte, North Carolina, USA

Full-time

Responsibilities: Lead the development and implementation of submission-ready SDTM datasets in accordance with regulatory requirements (e.g., FDA, EMA, PMDA). Collaborate with regulatory affairs and quality assurance teams to ensure compliance with submission guidelines and standards. Perform thorough quality control checks to validate the accuracy and completeness of submission datasets. Coordinate the preparation and documentation of submission packages, including data specifications and v

Practice Director-Biostatistics

IKCON TECHNOLOGIES Inc.

New Jersey, USA

Contract

IKCON PHARMA INC delivers exceptional IT services and solutions that provide clients with a definite edge over competitors and promote the highest standards of quality. We are currently looking for Practice Director-Biostatistics with one of our clients in Remote. If you are actively looking for opportunities, please send us your updated resume with your contact details. This is a remote position with the option of working from our corporate headquarters in South Plainfield, New Jersey. "U.S.

Associate Director, Data Monitoring Committee (DMC) Expert

Eli Lilly and Company

Remote or Indianapolis, Indiana, USA

Full-time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined