ecw clinical trainer Jobs

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Clinical Editing Coding Analyst | Remote | ContractJob Title - Clinical Editing Coding Analyst | Remote | Contract

Walker HealthforceCompany Name - Walker Healthforce

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Remote

Contract

Clinical Editing Coding Analyst |Remote |Contract Walker Healthforce is seeking a Clinical Editing Coding Analyst with 1-5+ years of experience.. This is a 6-month contract opportunity. CORE REQUIREMENTS: Certified Professional Codercertification (e.g., CPC, CCS, CCS-P, or RHIT) 1-5 years experience - in billing/coding (preferably in a comprehensive surgical center or facility) or Claims resolution (including adjudication, coding, thorough analysis and problem-solving) Ability to analyze, inves

Business Analyst ( BA with Clinical Experience)Job Title - Business Analyst ( BA with Clinical Experience)

SwanktekCompany Name - Swanktek

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North Chicago, Illinois, USA

Full-time

BA with Clinical ExperienceLocation: North Chicago, IL (Hybrid) Overall - 12+ years JD Minimum 10 years of BA experienceLS R&D projects experience in IT engagementsExtensive domain experience in Clinical Development Operations and Data GxP knowledge and experience of working in Regulated environmentUnderstanding of SDLC processesStrong business facing communication skillsUse of Jira and Confluence, exp on Agile methodologies

Clinical EMR Systems AnalystJob Title - Clinical EMR Systems Analyst

Vaco by HighspringCompany Name - Vaco by Highspring

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Columbus, Ohio, USA

Full-time

Direct Hire - Local to Columbus, OH Cannot provide Sponsorship at this time Compensation $60,000 - $70,000 dependent upon experience The Senior Clinical Systems Analyst serves as the lead implementation and support person for all clinical applications and facilitates the configuration, implementation, and training of the electronic medical record and other clinical computer software. The Senior Clinical Systems Analyst is a subject matter expert assisting in the resolution of issues affecting a

Clinical Data managerJob Title - Clinical Data manager

Intone Networks Inc.Company Name - Intone Networks Inc.

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Remote

Third Party, Contract

Need stronger with working on Data Acquisition, DTAs and vendor relations. Responsibilities: Support the planning, setup, and acquisition of external clinical data at the study level, assisting in managing study start-up, conduct, and closeout activities.Assist in creating external data transfer agreements, ensuring alignment with Takeda Standards and specifications to support data integration, analysis, and reporting.Provide support in setting up infrastructure for external data to flow into T

Clinical Laboratory Scientist II (CLS) -GeneralistJob Title - Clinical Laboratory Scientist II (CLS) -Generalist

Power PersonnelCompany Name - Power Personnel

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San Jose, California, USA

Full-time

Job DescriptionJob Description Here is the enhanced and refined job description for the Clinical Laboratory Scientist II (CLS) - Generalist position: Elevator PitchAre you a Clinical Laboratory Scientist and want to gain experience at one of the nation's top teaching Hospitals? Join now! Want to gain world-leading experience in CLS? Join now! About the Job Pay Rate: $105.00Location: 225 N Jackson Avenue, San Jose, CA 95116Schedule: 5 days a week, alternating weekendsShift details: 11:00pm-7:30

Clinical Business/Data Analyst - NYC (onsite)Job Title - Clinical Business/Data Analyst - NYC (onsite)

Winston Staffing ServiceCompany Name - Winston Staffing Service

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New York, New York, USA

Contract

This position requires onsite, 5 days a week, Monday Friday in Downtown, NYC. This Role will be 100% on site with potential to hire. If hired, it will be 2 days at home and 3 days in office. Interviews will be Virtual and only PREA required. Previous experience working with Clinical Data a must **NO AGENCIES, NO EMPLOYERS, NO 1099, NO C2C Must have year of experience gathering and documenting business, clinical, and/or functional requirements for software applications development and implement

Clinical Communications Analyst - IDAR Experienced EngineerJob Title - Clinical Communications Analyst - IDAR Experienced Engineer

Johnson & JohnsonCompany Name - Johnson & Johnson

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Remote or 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

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

Clinical SAS programmerJob Title - Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Chicago, Illinois, USA

Full-time

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. Attending multi-disciplinary team meetings, representing the programming function. Develop software systems to generate displays of clinal al study

Clinical SAS programmerJob Title - Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Omaha, Nebraska, 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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Hartford, Connecticut, 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 SAS programmerJob Title - Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Cambridge, Massachusetts, USA

Full-time

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. Attending multi-disciplinary team meetings, representing the programmi

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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Dallas, Texas, USA

Full-time

Clinical Data SpecialistJob Title - Clinical Data Specialist

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Illinois, USA

Full-time

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

Clinical SAS programmerJob Title - Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Athens, Georgia, USA

Full-time

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Newark, New Jersey, USA

Full-time

Sr. Clinical SAS ProgrammerJob Title - Sr. Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Newark, New Jersey, 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. Fulfill ad-hoc analysis requests. Provide other services. Requirements: Ba

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Minneapolis, Minnesota, 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 Data SpecialistJob Title - Clinical Data Specialist

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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San Diego, California, USA

Full-time

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 o