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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

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 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 Application Administrator Support IIJob Title - Clinical Application Administrator Support II

Bravo Technical ResourcesCompany Name - Bravo Technical Resources

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Addison, Texas, USA

Full-time

The Support Engineer II, Clinical Apps The Clinical Applications Support Engineer II will provide second-level support for clinical applications and EHR systems used in occupational medicine. This position ensures optimal performance, availability, and integration of patient management platforms and connected devices. The role collaborates with IT teams, clinical staff, and third-party vendors to resolve issues, ensure security compliance, and deliver excellent service to end users. Key Respons

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 User Experience and Endpoint LeadJob Title - Clinical User Experience and Endpoint Lead

Innova Solutions, IncCompany Name - Innova Solutions, Inc

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Fredericton, New Brunswick, Canada

Contract

A client of Innova Solutions is immediately hiring for a Clinical User Experience and Endpoint Lead. Position type: Contract Location: Fredericton, New Brunswick, Canada As a Clinical User Experience and Endpoint Lead, you will be responsible for: Description: A Bachelor s level University degree in Computer Science, Business Administration, Healthcare or a similar discipline.Demonstrated experience in a user experience leadership role on at least one major Clinical Information System implemen

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

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

B2B Healthcare/Clinical Solutions Product Marketing ManagerJob Title - B2B Healthcare/Clinical Solutions Product Marketing Manager

U.S. Tech Solutions Inc.Company Name - U.S. Tech Solutions Inc.

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San Bruno, California, USA

Contract

Job Description: We are looking for a creative, analytical, and detail-oriented Product Marketing Associate to join our growing team.This role is ideal for someone with a background in strategy consulting or product marketing, particularly in the healthcare, life sciences, or pharmaceutical industries.The successful candidate will play a key role in creating high-impact presentation materials that support strategic commercial opportunities across client diverse product portfolio.Reporting to the

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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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

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Austin, Texas, 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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Newark, New Jersey, USA

Full-time

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

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 SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Hartford, Connecticut, USA

Full-time

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 Supply Systems AdministratorJob Title - Clinical Supply Systems Administrator

Johnson & JohnsonCompany Name - Johnson & Johnson

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Remote or Malvern, 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

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

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