CDISC jobs

Piscataway, New Jersey

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6d ago

Job title: Statistical Analysts Rang Technologies Inc has openings for Statistical Analysts in Piscataway, NJ and other unanticipated locations nationwide. Duties: Quality Control (source code review, double-programming, and log review) and edit checks using various SAS procedures and macro facility. Review SDTM mapping documents and SDTM data to assure the traceability from raw data source. Perform efficacy analysis on primary and secondary endpoints testing the clinical trials hypotheses and

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Full-time

Depends on Experience

Programmer Analyst II

San Diego, California

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Today

Location: San Diego, CA Schedule: Hybrid (3 days per week in the office) The Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute comprised of an expert group of scientific collaborators committed to advancing the development of new treatments for Alzheimer's Disease (AD) through innovative clinical trials. We are seeking a Programmer Analyst II to join our growing team. This role is ideal for a motivated develop

Full-time

USD 43.72 - 58.71 per hour

Senior Clinical Data Analyst

Warsaw, Indiana

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Today

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

Full-time

USD 89,000.00 - 140,000.00 per year

Sr Clinical Data Scientist (Data Mgr)

No location provided

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Today

Job Description Summary #LI-Hybrid Location: East Hanover, NJ This key role will use advanced data management tools and techniques, provide professional and lean execution of Data Management products and milestones with respect to cost, quality and timelines for all assigned trials within Clinical Data Acquisition and Management. In addition, they will ensure consistently high-quality data delivery (in alignment with the Novartis Clinical Data Quality Statement) to analysis and reporting. Job

Full-time

USD 94,000.00 - 174,000.00 per year

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).

Full-time

Sr. Clinical SAS Programmer

Newark, New Jersey

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Today

Responsibilities: Perform data manipulation, analysis, and reporting of clinical trial data. Develop and maintain department/system-level macros. Create and review SDTM and ADaM specifications. Create and validate SDTM data sets. Create and validate analysis data sets. Create and validate patient profiles. Program and generate tables, figures, and listings (TFLs). Validate and document SAS programs and outputs. Fulfill ad-hoc analysis requests. Provide other services. Requirements: Ba

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. Attending multi-disciplinary team meetings, representing the programming function. Develop software systems to generate displays of clinal al study

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. Attending multi-disciplinary team meetings, representing the programmi

Full-time

Clinical SAS Programmer

Austin, Texas

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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

Sr. SAS Programmer

Durham, North Carolina

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Today

Responsibilities: The Sr. SAS Programmer will be responsible for statistical programming for the client's clinical studies. In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to project team members. Our Ideal candidate will have a strong work ethic capable of thriving in a high growth, fast paced and intellectual environment. Serves as lead programmer for assigned projects to provide statistical and programming support i

Full-time

Clinical SAS programmer

Omaha, Nebraska

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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 p

Full-time

Clinical SAS Programmer

Hartford, Connecticut

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Today

Full-time

Clinical SAS Programmer

Minneapolis, Minnesota

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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

Newark, New Jersey

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Today

Full-time

Clinical SAS programmer

Athens, Georgia

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Today

Full-time

Clinical SAS programmer

Dallas, Texas

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Today

Full-time

Clinical SAS Programmer

Princeton, New Jersey

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Today

Full-time

Clinical SAS Programmer

Edison, New Jersey

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Today

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

Full-time

Senior SAS Programmer

Seattle, Washington

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Today

Responsibilities: The Senior SAS Programmer will be responsible for statistical programming for the client's clinical studies. In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to project team members. Our Ideal candidate will have a strong work ethic capable of thriving in a high growth, fast paced and intellectual environment. Serves as lead programmer for assigned projects to provide statistical and programming suppor

Full-time

Senior SAS Programmer

Albany, New York

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Today

Responsibilities: Design, code, and test SAS programs used to generate CDISC SDTM & ADaM domains and tables, listings & figures outputs. Perform analyses defined in the statistical analysis plan as well as ad hoc analyses as requested. Validate CDISC SDTM and ADaM data sets by using Open-CDISC Validation Tool. Design, code and test SAS macro libraries to be used for development standardization. Create data definition documents for CDISC SDTM and ADaM datasets and other electronic submission

Full-time

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