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SAS Clinical Programmer

INGENworks

•

Remote

Contract

Job Title: SAS Clinical Programmer Location: West Point, PA Area (Remote) (w2)EXP - 5 years | Any Visa Job SummaryOVERALL RESPONSIBILITIES: Development and generation of SAS analysis datasets, tables, listings, and graphs from assigned clinical sources; leading development and maintenance of associated operating procedures; and participating in external industry forums (e.g., CDISC, SCDM, and User Groups). This individual performs with minimal on moderately difficult deliverables. POSITION DUTI
Easy Apply
Posted 1 day ago

SAS Clinical Programmer

INGENworks

•

Remote

Contract

Job Title: SAS Clinical Programmer Location: West Point, PA Area (Remote) (w2)EXP - 2-3 yearsFunctional and Technical Competencies:Proficiency in Base SAS, SAS/STAT and SAS Macro language. Advanced SAS certification desirable. Experience programming with R desirable.Demonstrated ability to work in teams to deliver critical milestones.Experience with CDISC datasets, tables, listings and figures desirable.Excellent verbal and written communication skills Leadership Competencies: Connect Participat
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Posted 1 day ago | Updated 1 day ago

Sr. Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Indianapolis, Indiana, USA

Full-time

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. Fulfil ad-hoc analysis requests. Provide other services. Requirements: Bachelor's deg
Posted 4 days ago | Updated 11 hours ago

SAS Programmer

Katalyst Healthcares and Lifesciences

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Edison, New Jersey, USA

Full-time

Responsibilities: Provide support for all aspects of reporting including report development, maintenance, and documentation. Develop, test, debug, and deploy the SAS programs. Develop statistical analysis using standard reporting, ad hoc reporting, and data statistics. Develop SAS and SQL queries to pull the data translated from a database diagram and report requirements, Work with large data sets and cleanse data to integrity. Deliver timely and accurate output in a variety of different fo
Posted 17 days ago | Updated 11 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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Irving, Texas, USA

Full-time

Responsibilities: Performing data manipulation, analysis, and reporting of clinical trial data for both safety and efficacy (ISS/Client) utilizing SAS programming. Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs). Production and QC / validation programming. Ability to program from scratch and able to handle complicated domains and TLF's. Ability to read and apply protocol and SAP. Demonstrate good understanding of the endpoints and d
Posted 17 days ago | Updated 11 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Boston, Massachusetts, USA

Full-time

Responsibilities: Attending multi-disciplinary team meetings, representing the programming function. 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. Develop software systems to generate displays of clinal all stu
Posted 17 days ago | Updated 11 hours ago

SAS Programmer

Katalyst Healthcares and Lifesciences

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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.
Posted 8 days ago | Updated 11 hours ago

Senior SAS Programmer

Katalyst Healthcares and Lifesciences

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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
Posted 17 days ago | Updated 11 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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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
Posted 17 days ago | Updated 11 hours ago

Senior Manager Data Management

Katalyst Healthcares and Lifesciences

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San Diego, California, USA

Full-time

Responsibilities: Responsible for data management documentation, including, but not limited to data management plan(DMP), CRF, eCRF design, edit check specifications, data issue logs, and data review plans and ensures all documents follow study design and regulatory requirements. Maintain Data Management outsourcing metrics and key performance indicators to aid the selection of CRO partners / Vendors and the ongoing management of partnerships. Participate in vendor qualifications and audits.
Posted 17 days ago | Updated 11 hours ago

SAS Clinical Trails Programmer

Katalyst Healthcares and Lifesciences

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Cary, North Carolina, USA

Full-time

Responsibilities: The consultant will provide programming/analytical support utilizing client as the primary programming language to create and manage the production of analysis reports. summary tables/listings and graphs for clinical trials submitted to various regulatory bodies worldwide. The consultant must have excellent communication skills and must be able to communicate about the techniques developed and results of analysis both to executives and other analysts in the organization. Pe
Posted 17 days ago | Updated 11 hours ago

Prin Clin Data Scientist (Data Mgr)

Novartis

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Hanover

Full-time

Job Description Summary Location: East Hanover, NJ Onsite (cannot be done remotely) Hiring for multiple roles. About the role: Love clinical data management? Bring that passion to Novartis! This key Principal Clinical Data Scientist will be responsible and accountable for managing all Data Management deliverables at a consistently high standard with respect to cost, quality, and timelines for all assigned indications within one or more Global Clinical Program(s)/Project(s). Job Description
Posted 41 days ago | Updated 11 hours ago

Senior Consultant - Clinical Data Programming

Veeva Systems

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Raleigh, North Carolina, USA

Full-time

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company - we made history in 2021 by becoming a public benefit corporation
Posted 21 days ago | Updated 11 hours ago

Associate Director, Scientific Reference Data and Ontologies

Merck & Company Inc

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Remote or Rahway, New Jersey, USA

Full-time

Job Description The Associate Director of Scientific Nomenclature and Reference Data is responsible for assigning accurate chemical nomenclature to small molecules and biologics, as well as creating and maintaining reference data utilized across the company. The incumbent will play a pivotal role in meeting cross-divisional and regulatory requirements by their strong scientific background, excellent communications skills, and project management skills to derive high-quality reference data to me
Posted 60+ days ago | Updated 11 hours ago

Assoicate Director of Clinical Data Science

Pivotal Solutions Inc

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Menlo Park, California, USA

Full-time

Qualifications Required: Master s or PhD in Data Science, Biostatistics, Computer Science, Life Sciences, or a related field10+ years of experience in clinical data programming or clinical data science within a pharmaceutical, biotech, or CRO environmentProficiency in R, SAS, or Python, and experience with data visualization tools (e.g., Shiny, Spotfire, Tableau)Strong understanding of clinical data standards (e.g., CDISC, SDTM) and clinical trial processesDemonstrated ability to collaborate wi
Easy Apply
Posted 22 days ago

Clinical Data Manager

Tandym Tech

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Remote

Contract

A recognized pharmaceutical company has a great Remote opportunity awaiting a new Clinical Data Manager. In this role, the Clinical Data Manager will be responsible for contributing Data Management Support for assigned programs. The contractor is a self-motivated, collaborative clinical data management professional who is a self-starter and thrives in a fast-paced environment. Responsibilities: Work with the Clinical Data Management (CDM) Lead to support operational activities for one or more pr
Easy Apply
Posted 22 days ago | Updated moments ago

SAS Developer

Princeton IT Services

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Princeton, New Jersey, USA

Contract

Job Title: SAS Developer Location: Princeton, NJ (Onsite) Job Type: Full-Time Contract Job Summary: We are seeking a highly skilled and detail-oriented SAS Developer to join our data analytics and reporting team in Princeton, NJ. The ideal candidate will have deep expertise in SAS programming and data manipulation, along with experience working in healthcare, life sciences, or financial services. This role involves working with large datasets, generating statistical reports, and supporting e