CDISC jobs

Jersey City, New Jersey

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3d ago

Job Title: Senior Medidata Consultant / Developer (EDC & Coder) Location: Onsite New Jersey, US Position Overview We are seeking a Senior Medidata Consultant / Developer with extensive experience in Medidata EDC (Rave) and Medidata Coder platforms to support, enhance, and optimize clinical trial data management systems. The ideal candidate will possess a strong understanding of clinical data workflows, along with solid technical troubleshooting, configuration, and integration expertise. This rol

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Full-time

$0+

Senior Medidata Consultant / Developer (EDC & Coder)

Jersey City, New Jersey

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4d ago

Job Title: Senior Medidata Consultant / Developer (EDC & Coder) Location: Onsite New Jersey, US Experience Level: 6 10 years Employment Type: Full-Time Position Overview We are seeking a Senior Medidata Consultant / Developer with extensive experience in Medidata EDC (Rave) and Medidata Coder platforms to support, enhance, and optimize clinical trial data management systems. The ideal candidate will possess a strong understanding of clinical data workflows, along with solid technical troubleshoo

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Full-time

Depends on Experience

Senior Medidata Consultant / Developer (EDC & Coder)

Jersey City, New Jersey

•

Today

Position Overview We are seeking a Senior Medidata Consultant / Developer with extensive experience in Medidata EDC (Rave) and Medidata Coder platforms to support, enhance, and optimize clinical trial data management systems. The ideal candidate will possess a strong understanding of clinical data workflows, along with solid technical troubleshooting, configuration, and integration expertise. This role involves close collaboration with global clinical operations, data management, and IT t

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Contract

Senior Medidata Consultant / Developer (EDC & Coder)

New Brunswick, New Jersey

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Yesterday

Job Title: Senior Medidata Consultant / Developer (EDC & Coder) Location : New Brunswick, NJ Experience Level: 6 10 years Employment Type: Full-Time / Contract Position Overview We are seeking a Senior Medidata Consultant / Developer with extensive experience in Medidata EDC (Rave) and Medidata Coder platforms to support, enhance, and optimize clinical trial data management systems. The ideal candidate will possess a strong understanding of clinical data workflows, along with solid

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Full-time, Part-time, Contract, Third Party

SAS Programmer

Remote or Warsaw, Masovian Voivodeship

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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

Sr. SAS Programmer

Wilmington, Delaware

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Today

Job Description: The Sr. SAS Programmer provides PKPD programming aspects of pharmacokinetics, pharmacodynamics data management by timely completion and high quality of all required deliverables. Responsibilities: Prepare data for state-of-the-art analysis, such as PPK, PKPD, exposure-response (efficacy or safety), and C-QTc, typically based on CDISC ADaM / SDTM datasets. Prepare data for state-of-the-art NCA analysis, such as ADPC, PP, and ADPP, including the creation of defined packages and r

Full-time

Clinical Data Engineering Lead

Cambridge, England

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Today

Job Description Summary About the role: #LI:Onsite Are you ready to make a lasting impact by building the future of oncology research? Novartis Biomedical Research (NBR) is searching for a visionary Associate Director to lead Clinical Data Engineering within our Oncology Data Science (OncDS) team. In this pivotal role, you'll be at the forefront of shaping early clinical development by building innovative biomarker data infrastructure, championing translational research, unlocking AI-powered d

Full-time

USD 176,400.00 - 327,600.00 per year

Director, R&D Data Science, Data Products - Global Development

Remote or Hopewell Township, New Jersey

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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

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

SAS Programmer

New Jersey

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Today

Responsibilities: You'll be at the forefront of developing and validating programs that create datasets conforming to CDISC standards. Your expertise will drive the creation of Tables, Listings, and Figures for analysis purposes. Depending on the complexity of the study, you may lead programming projects, ensuring adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. You'll also have the opportunity to mentor junior programmers and represent Statistical Programming i

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

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

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

Data Standards Manager III

North Chicago, Illinois

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Today

Responsibilities: Maintains complete and in-depth understanding of all CDISC guidance documents and implementation guides as well as FDA guidance and regulation regarding electronic submission of data. Keeps abreast of industry trends in data mapping, data management, standards compliance methodologies, metadata management and data warehousing. eCRF Design - Demonstrates extensive understanding of CDASH and SDTM standards and concepts. ble to critically review eCRF designs to ensure compatibilit

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

SAS Programmer

Omaha, Nebraska

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Today

Roles & Responsibilities: Bachelor's degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, or related applicable field. Minimum of 5 to 8 years' SAS programming experience in the pharmaceutical/biotech industry with some experience using CDISC standards. Create source and validation programs using SAS software for SDTM datasets, analysis datasets, and tables, listings, and graphs (TLGs) for multiple studies/products. Integrates data across

Full-time

Clinical SAS Programmer

Detroit, Michigan

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Today

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

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

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

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