field clinical engineer Jobs

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Sr. Clinical SAS programmerJob Title - Sr. Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Computer System Validation Analyst - R Studio & Clinical SystemsJob Title - Computer System Validation Analyst - R Studio & Clinical Systems

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Remote or New Jersey, USA

Full-time

Responsibilities: Lead validation planning, risk assessment, and execution for R Studio, GitLab, and Medidata Rave EDC. Develop and execute validation documentation including: Validation Plans (VP.). User Requirements Specifications (URS.). Risk Assessments (RA.). Functional and Design Specifications. Traceability Matrix (RTM.). Test Protocols (IQ/OQ/PQ or CSA-based scripts.). Validation Summary Reports (VSR.). Collaborate with cross-functional stakeholders including Clinical Data Mana

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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South San Francisco, California, USA

Full-time

Responsibilities: Performs all SAS programming required for clinical trial analysis and reporting. Ensures that activities and processes performed are conducted according to sponsor requirements. Works closely with the Biostatistics and Data Management departments on various clinical projects. Designs and/or reviews database structure. Writes edit checks from the Data Cleaning Plan (DCP) specifications. Creates derived-analysis datasets. Executes analyses specified in the Statistical Anal

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Princeton, New Jersey, 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.

Clinical Systems Analyst TrizettoJob Title - Clinical Systems Analyst Trizetto

Tech Pro Inc.Company Name - Tech Pro Inc.

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Remote

Contract

send your resume directly to my email kumar @ techpro-inc . com with Subject: Applying from Dice (only this line) OR click on Apply now Job Description: Configuration Management and Content Specialist Configuration Management Documentation: Create comprehensive documentation of configuration management processes. Develop process flowcharts for configuration management. Write step-by-step setup and testing procedures. Prepare troubleshooting guides for common issues. Document version control a

Senior Consultant - Clinical Data ProgrammingJob Title - Senior Consultant - Clinical Data Programming

Veeva SystemsCompany Name - 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

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Clinical Data AnalystJob Title - Clinical Data Analyst

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Irvine, California, USA

Full-time

Responsibilities: The main function of a clinical data analyst is to create moderately complex metrics to identify trends in data and remediation, utilizing tools (e.g., systems, reports) to assess the need for training and provide basic recommendations to improve data status during study conduct. Evaluate data errors and collection issues; provide guidance and recommendations to the clinical team for resolution. Define and specify clinically data collection requirements (e.g., eCRFs, CRFs, ed

Clinical Services Project ManagerJob Title - Clinical Services Project Manager

Software Guidance & AssistanceCompany Name - Software Guidance & Assistance

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Tucson, Arizona, USA

Contract

Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Services Project Manager for a contract assignment with one of our premier Pharmaceutical clients in Tucson, AZ. Responsibilities : Manages multiple clinical and lab services projects of less complex nature from initiation through contract completion. Applies project management skills and experience in delivering projects on time, within budget and with high customer satisfaction. Facilitates cross-functional interacti

Clinical Business System Analyst - Healthcare, Trizetto Communication SystemJob Title - Clinical Business System Analyst - Healthcare, Trizetto Communication System

People Force Consulting IncCompany Name - People Force Consulting Inc

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Remote

Contract

As an Clinical Business System Analyst, you will be a part of an Agile team to build healthcare applications and implement new features while adhering to the best coding development standards . Responsibilities: - Configuration Management Documentation: Create comprehensive documentation of configuration management processes.Develop process flowcharts for configuration management.Write step-by-step set-up and testing procedures.Prepare troubleshooting guides for common issues.Document version co

Clinical SAS programmerJob Title - Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Senior Clinical Data AnalystJob Title - Senior Clinical Data Analyst

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Boston, Massachusetts, USA

Full-time

Job Description: This position focuses on assisting with analysing data and deriving insights from clinical and safety data sources to generate evidence and support decision making across the organization. The Associate will leverage a variety of analytics and visualization techniques to contribute to research, clinical development, drug safety and post-marketing activities. Responsibilities: Collaborates and works closely with cross-functional teams, including data analysts/engineers and busin

Clinical Supply Systems AdministratorJob Title - Clinical Supply Systems Administrator

Johnson & JohnsonCompany Name - Johnson & Johnson

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Remote or Horsham, Pennsylvania, USA

Full-time

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

QA Clinical Supplies SpecialistJob Title - QA Clinical Supplies Specialist

Zachary Piper Solutions, LLCCompany Name - Zachary Piper Solutions, LLC

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Lansdale, Pennsylvania, USA

Full-time

Piper Companies is seeking a QA Clinical Supplies Specialist to join a major pharmaceutical manufacturing company located in Lansdale, PA. This is a Hybrid role. The QA Clinical Supplies Specialist will ensure the quality, compliance and integrity of clinical trial supplies. Responsibilities of the QA Clinical Supplies Specialist include: Ensure clinical supply materials meet company policies and regulatory standards. Lead projects aimed at improving process performance, including yiel

IT Consultant V, Solutions - SNOMED CT, Clinical Coding, EHRJob Title - IT Consultant V, Solutions - SNOMED CT, Clinical Coding, EHR

Kaiser PermanenteCompany Name - Kaiser Permanente

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Pleasanton, California, USA

Full-time

Job Summary: The Concergent Data Modeler within the Convergent Medical Terminology team (CMT) is responsible for designing, maintaining, and optimizing clinical terminology models using SNOMED CT (Systematized Nomenclature of Medicine - Clinical Terms). This role supports interoperability, data normalization, and semantic precision in electronic health records (EHRs), clinical research, and healthcare analytics. The ideal candidate has a strong understanding of clinical terminology systems, ont

Data Scientist, Multimodal Data & Analytics in Clinical DevelopmentJob Title - Data Scientist, Multimodal Data & Analytics in Clinical Development

NovartisCompany Name - Novartis

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Cambridge, England, United Kingdom

Full-time

Job Description Summary The Multimodal Data and Analytics group in Advanced Quantitative Sciences, Novartis Development is searching for a Data Scientist to support the design and hands-on execution of modeling strategies using patient-level -omics, imaging and clinical outcomes data. As part of interdisciplinary drug development teams, your work will influence development decisions and inform late phase trials and regulatory submissions. Your focus will be on combining your domain knowledge of

Clinical Data AssociateJob Title - Clinical Data Associate

Eli Lilly and CompanyCompany Name - Eli Lilly and Company

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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

Data Owner - Manager, Clinical Supply Chain DataJob Title - Data Owner - Manager, Clinical Supply Chain Data

Johnson & JohnsonCompany Name - Johnson & Johnson

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Remote or Hopewell Township, New Jersey, USA

Full-time

Clinical Provider Account ManagerJob Title - Clinical Provider Account Manager

Pegasus Knowledge SolutionsCompany Name - Pegasus Knowledge Solutions

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Remote

Full-time

Responsibilities: The Clinical Provider Account Manager is responsible for building and maintaining strong relationships with assigned providers, acting as their main point of contact to address inquiries, resolve issues, and ensure high-quality service delivery. Key responsibilities include: Client Relationship Management: Strengthening provider relationships, managing communication, and mitigating risks.Account Management: Overseeing provider satisfaction, implementing new sites and services,