CDISC Jobs

Refine Results
1 - 20 of 20 Jobs

Associate Director - Data Standards

Eli Lilly and Company

•

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
Posted 22 days ago | Updated 3 hours ago

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
Posted 12 days ago | Updated 3 hours ago

SAS Programmer

Katalyst Healthcares and Lifesciences

•

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 47 days ago | Updated 3 hours ago

Sr. Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

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 34 days ago | Updated 3 hours ago

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
Posted 42 days ago | Updated 3 hours ago

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
Posted 4 days ago | Updated 3 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

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 47 days ago | Updated 3 hours ago

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
Posted 22 days ago | Updated 3 hours ago

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
Posted 8 days ago | Updated 3 hours ago

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.
Posted 38 days ago | Updated 3 hours ago

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
Posted 47 days ago | Updated 3 hours ago

Senior Manager Data Management

Katalyst Healthcares and Lifesciences

•

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 47 days ago | Updated 3 hours ago

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
Posted 47 days ago | Updated 3 hours ago

SAS Clinical Trails Programmer

Katalyst Healthcares and Lifesciences

•

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 47 days ago | Updated 3 hours ago

Prin Clin Data Scientist (Data Mgr)

Novartis

•

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 60+ days ago | Updated 3 hours ago

Senior Consultant - Clinical Data Programming

Veeva Systems

•

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 51 days ago | Updated 3 hours ago

Clinical Data Manager

Tandym Tech

•

Woburn, Massachusetts, USA

Contract

A pharmaceutical company in Massachusetts is currently seeking a new Clinical Data Manager to provide Data Management support for assigned programs. Responsibilities: Work with Clinical Data Management (CDM) Lead to support operational activities for one or more programs Monitor data management vendor quality of work through key performance metrics Maintain program level DM deliverable timelines in accordance with program development strategy Support data management at cross-functional team mee
Easy Apply
Posted 15 days ago | Updated 8 hours ago

Statistical Analysts

Rang Technologies Inc.

•

Piscataway, New Jersey, USA

Full-time

Job title: Statistical Analysts Rang Technologies Inc has openings for Statistical Analysts in Piscataway, NJ and other unanticipated locations nationwide. Duties: Perform quality control checks and edit checks using standard procedures and existing macros. Determine whether the right statistical approach is being used to analyze the data to answer the research question. Generate statistical results, using listings, figures, and tables for presentation at conferences and for publication in peer-
Easy Apply
Posted 16 hours ago

Statistical Programmer Consultant

Tandym Tech

•

Novato, California, USA

Contract

Our client, a leading Life Sciences Company, needs to hire a Statistical Programmer to provide programming support for Phase 1 to Phase 3 studies, including project integration and disease monitoring project work. This is a 6-month contract, 100% REMOTE. **Qualified candidates must be able to work on a W2 basis. Responsibilities: Provides timely support to the project team on all statistical programming matters according to the project strategy. Programs SDTM/ADaM/TLFs for the studies, write
Easy Apply
Posted 26 days ago | Updated 8 hours ago

AVP Data Strategy & Governance

New Millennium Consulting

•

Philadelphia, Pennsylvania, USA

Full-time

Job title: AVP Data Strategy & Governance Job location: Philadelphia, PA Job type: Full time Key Focus: Microsoft Azure, Microsoft Fabric, NIST 800-171, HIPAA A leading healthcare is seeking an Associate Vice President Data Strategy & Governance. The AVP Data Strategy & Governance will serve as the executive leader responsible for shaping and executing the enterprise-wide data vision. This role will oversee the strategic direction, architecture, governance, and compliance of the organization s d