junior sas clinical programmer jobs

Remote or Pennsylvania

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Today

Stefanini Group is hiring! Stefanini is looking for Clinical Programmer - (Israel Based - Fully Remote) For quick apply, please reach out to Ranjit Kumar - call: / Email: **This is a fully remote position for a Clinical Programmer - Israel Based - Fully Remote ** Shift Schedule: 8:00am - 5:00 pm Sunday - Thursday Israel time Core essential:Minimal Bachelor's degree in any fieldMinimal 5 years experience with Clinical data, SDTM IG, and Pinnacle 21. Position Summary:The Clinical Programming Manag

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Contract

$60 - $69 /hr

Principal Statistician Programmer

Remote or West Chester, Pennsylvania

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Today

Stefanini Group is hiring!Stefanini is looking for Principal Statistician Programmer for 100% Remote work.For quick Apply, please reach out to Ranjit Kumar- call: /email: for W2 Candidates only! Provide statistical support in protocol development for observational studies and/or clinical trials.Author and review of statistical analysis plans, analysis dataset specifications, and TFL shells.Work with programming and other cross-functional teams in Phase-4 non-interventional study to develop CRF,

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Contract

$84 - $98 /hr

SAS Programmer

Remote or Warsaw, Indiana

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Today

Stefanini Group is hiring!Stefanini is looking for SAS Programmers for 100% Remote work in Poland.For quick Apply, please reach out to Ghanshyam Sharma- / Shift Schedule: Day Shift The Statistical Programming Contractor 3 is responsible for providing comprehensive programming support, including managing the timely and accurate execution of programming components of clinical trials.The statistical programming contractor independently manages completed projects that involve global tasks, or cross

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Contract

Market

Biostatistician/SAS

Remote

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16d ago

Position: Biostatistician -Open Position-HI Type: contract Duration: 12 months Location: Hawai Responsibilities. Write/review SAP and clinical trial protocol; develop and validate complex statistical models and SAS programs for analysis, management & reporting of clinical data. Perform statistical analysis, create and verify clinical trial reports and TLGs to support FDA submission. Req.: Master's degree/equiv. in Biostatistics, Statistics, Public Health or related. Proficiency in clinical dat

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Contract

Depends on Experience

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.

Full-time

Clinical SAS Programmer

Detroit, Michigan

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Today

Full-time

Clinical SAS Programmer

Austin, Texas

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Today

Full-time

Clinical SAS Programmer

Boulder, Colorado

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Today

Full-time

Clinical SAS Programmer

Chicago, Illinois

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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

Clinical SAS Programmer

Irvine, California

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Today

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 progra

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

Clinical SAS programmer

Lake Success, New York

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Today

Full-time

Clinical SAS Programmer

Worcester, Massachusetts

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Today

Responsibilities: Review protocols for CDISC conformance. Review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements. Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emme's' SDTM Implementation Guide, project standards, and the study protocol. Create DEFINE specifications for mapping of SDTM and ADaM compliant datasets. Review and QC submission ready SDTM datasets, define.xml, and supporting documentation, as appropriate.

Full-time

Clinical SAS Programmer

Hartford, Connecticut

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Today

Full-time

SAS Programmer

Atlanta, Georgia

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Today

Responsibilities: The statistical programming contractor independently manages completed projects that involve global tasks, or cross functional teams. The role may require providing inputs to design and analysis, and reporting the results of clinical trials, including programming rules and mocked T/L/G In addition, providing programming support for publication for our marketed drugs Primarily works at the study, product / program level. Provides comprehensive programming support, including deve

Full-time

Clinical SAS programmer

Chicago, Illinois

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Today

Responsibilities: Create or review and approve programming plans at study and project level. Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.) Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies. ttending multi-disciplinary team meetings, representing the programming function. Develop software systems to generate displays of clinal al study data

Full-time

SAS Programmer

Austin, Texas

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Today

Responsibilities: The statistical programming contractor independently manages completed projects that involve global tasks, or cross functional teams. The role may require providing inputs to design and analysis, and reporting the results of clinical trials, including programming rules and mocked T/L/G. In addition, providing programming support for publication for our marketed drugs. Provides comprehensive programming support, including development of programs, ADaM specifications, analysis (d

Full-time

Clinical SAS Programmer

Newark, New Jersey

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Today

Full-time

Clinical SAS programmer

Cambridge, Massachusetts

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Today

Responsibilities: Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.). Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies. Develop software systems to generate displays of clinal al study data as tables, listings, and graphs for electronic submission to regulatory agencies. ttending multi-disciplinary team meetings, representing the programming fu

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

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junior sas clinical programmer jobs