clinical trials jobs

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

Clinical SAS Programmer

Boulder, Colorado

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Today

Responsibilities: Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget. Conduct hands-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results for internal and external audiences. Ensure all relevant deliverables including investigator brochures, publications, all regulatory submissions (

Full-time

Clinical SAS Programmer

Newark, New Jersey

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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. Perfo

Full-time

Clinical Data Specialist

Alameda, California

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Today

Job Description: This position will play a critical role in ensuring the ethical and responsible conduct of clinical trials to protect study participants from potential harm, safeguard the integrity of the trial. By identifying potential problems early, the clinical data specialist can help prevent serious adverse events and ensure that the trial results are reliable and informative. Perform responsibilities meeting project commitments and in compliance with applicable regulations, good clinical

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

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. Perf

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 in on

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 progra

Full-time

Clinical Screening Coordinator - Roseville, CA

Roseville, California

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Today

Great companies need great teams to propel their operations. Join the group that solves business challenges and enhances the way we work and grow. Working at Gainwell carries its rewards. You'll have an incredible opportunity to grow your career in a company that values your contributions and puts a premium on work flexibility, learning, and career development. Summary As a Clinical Screening Coordinator at Gainwell, contribute your skills as we harness the power of technology to help our clien

Full-time

USD 30,500.00 - 43,500.00 per year

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: Bachelor's de

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 comp

Full-time

Clinical SAS programmer

Dallas, Texas

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Today

Full-time

Clinical Data Specialist

Illinois

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Today

Responsibilities: Reporting to the Clinical Data Manager, you'll be responsible for the development of real-world data variables from structured and unstructured data sources, including designing data capture forms and supplemental procedures to instruct the abstraction process. You'll lead the execution of feasibility testing to de-risk data capture approaches and own the implementation of data validation checks to ensure data quality. In addition, you'll work alongside other team members on wa

Full-time

Clinical SAS Programmer

Princeton, New Jersey

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Today

Full-time

Clinical SAS Programmer

Los Angeles, California

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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 Emmes' 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. Provi

Full-time

Clinical SAS programmer

Athens, Georgia

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Today

Full-time

Associate Director, Small Molecule Process Engineering-Lilly Medicine Foundry

Lebanon, Indiana

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Today

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

Full-time

USD 118,500.00 - 173,800.00 per year

Senior Software Developer

Durham, North Carolina

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Today

Hiring a Senior Software Developer! Our client is seeking a Senior Software Developer to join their Team! The Position: The Senior Software Developer will contribute to the development and continuous modernization of our client s core logistics operations management system. Core responsibilities will include: Deeply committed to continuous improvement, refactoring, TDD and pair programming to achieve technical excellence and understand how this supports long-term customer value. Understand how

Easy Apply

Third Party, Contract

Senior Principal, Process Safety Engineer - Lilly Medicine Foundry

Lebanon, Indiana

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Today

Full-time

USD 111,000.00 - 162,800.00 per year

Document Specialist V

Sunnyvale, California

•

Yesterday

OP is currently looking for a Document Control Analyst who will support product programs by managing standard operating procedures, work instructions, forms, and all types of records from product concept through obsolescence for a leading social media company. The Document Control Analyst has knowledge and experience working in regulated environments (i.e., ISO 13485) and sufficient knowledge and experience to be able to operate with minimal supervision. You are flexible, responsive, detail-orie

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clinical trials jobs