ecw clinical trainer Jobs

41 - 60 of 239 Jobs

Clinical Data SpecialistJob Title - Clinical Data Specialist

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Alameda, California, USA

Full-time

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 clinica

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Boulder, Colorado, USA

Full-time

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 submission

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: 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

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

Clinical SAS programmerJob Title - Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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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

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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Lake Success, New York, USA

Full-time

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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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

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 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

Sr Clinical Data Scientist (Data Mgr)Job Title - Sr Clinical Data Scientist (Data Mgr)

NovartisCompany Name - Novartis

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Hanover

Full-time

Job Description Summary #LI-Hybrid Location: East Hanover, NJ This key role will use advanced data management tools and techniques, provide professional and lean execution of Data Management products and milestones with respect to cost, quality and timelines for all assigned trials within Clinical Data Acquisition and Management. In addition, they will ensure consistently high-quality data delivery (in alignment with the Novartis Clinical Data Quality Statement) to analysis and reporting. Job

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 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

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

Data Scientist IV - UF Clinical and Translational Science Institute (CTSI)Job Title - Data Scientist IV - UF Clinical and Translational Science Institute (CTSI)

University of FloridaCompany Name - University of Florida

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No location provided

Full-time

Data Scientist IV - UF Clinical and Translational Science Institute (CTSI) Job no: 524887 Work type: Staff Full-Time Location: Lake Categories: Allied Health, Grant or Research Administration, Health Care Administration/Support Department:29680302 - MD-CTSI-VILLAGES HEALTH CRC Classification Title: Data Scientist IV Job Description: The UF Health - Precision Health Research Center (PHRC) located in The Villages, FL, hosted within the Clinical and Translational Science Institute (CTSI) se

Clinical Project CoordinatorJob Title - Clinical Project Coordinator

Elegant Enterprise Wide SolutionsCompany Name - Elegant Enterprise Wide Solutions

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Johnston, Iowa, USA

Full-time, Third Party

About this Position: Job Title: Clinical Project Coordinator Requirements: Be knowledgeable of and maintain currency as required to accomplish the following: Perform service without direct supervision in accordance with all applicable regulatory requirements and as outlined within this PWS. The required computer data entry into all applicable systems, protocols and procedures. To make administrative and procedural decisions, judgments on sensitive/confidential issues, and maintain confidentiali

Clinical Psychologist - Presque Isle MEJob Title - Clinical Psychologist - Presque Isle ME

MRG ExamsCompany Name - MRG Exams

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Presque Isle, Maine, USA

Full-time

Job DescriptionJob DescriptionClinical Psychologist Veteran Disability Assessments We are seeking a dedicated Clinical Psychologist to join our team in performing medical assessments for U.S. Veterans as part of the VA's disability benefits process. In performing Disability Assessments, you will review behavioral health records electronically through a secure Web Portal and perform a comprehensive assessment in-person on each Veteran. Key Responsibilities: Conduct in-person disability assessm

Clinical Psychologist - Presque Isle MEJob Title - Clinical Psychologist - Presque Isle ME

MRG ExamsCompany Name - MRG Exams

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Washburn, Maine, USA

Full-time

Clinical Psychologist - Presque Isle MEJob Title - Clinical Psychologist - Presque Isle ME

MRG ExamsCompany Name - MRG Exams

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Westfield, Maine, USA

Full-time