junior clinical analyst Jobs

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Clinical Field Service EngineerJob Title - Clinical Field Service Engineer

Nityo Infotech CorporationCompany Name - Nityo Infotech Corporation

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Boston, Massachusetts, USA

Contract

Clinical Field Service Engineer Responsibilities: Conduct comprehensive inventory of clinical devices, including radiology modalities, as part of a network migration project to ensure accurate asset tracking and seamless integration into the new infrastructure.Update configuration settings on medical devices to ensure proper functionality and connectivity during a phased, site-by-site network migration.Respond to technical support requests and helpdesk tickets in a timely manner, ensuring resolu

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

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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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 Data Analytics LeaderJob Title - Clinical Data Analytics Leader

Software Guidance & AssistanceCompany Name - Software Guidance & Assistance

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South San Francisco, California, USA

Contract

Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Data Analytics Leader for a direct placement assignment with one of our premier Pharmaceutical Services clients in South San Francisco, CA. Responsibilities : The Data Analytics Leader (DAL) in Early Clinical Development (ECD) Data Intelligence team supports ECD study teams by delivering timely and high-quality analysis and real-time interactive visualizations. The DAL is an expert in data analysis and data insights, enabl

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

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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Newark, 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.

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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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 Research Data ScientistJob Title - Clinical Research Data Scientist

Virginia JobsCompany Name - Virginia Jobs

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Richmond, Virginia, USA

Full-time

Mission or Goal of Unit: We champion health and well-being through the power of nursing education, discovery and practice. Chief Purpose of this position: The Clinical Research Data Scientist in the VCU SON will lead data management and computational efforts across multiple clinical research studies. The individual in this role will have advanced scripting and programming capabilities as well as expertise in research study design, data quality assurance, and analysis. The ideal candidate is hi

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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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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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 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

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 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 Documentation Coordinator CDIJob Title - Clinical Documentation Coordinator CDI

Pyramid Consulting, Inc.Company Name - Pyramid Consulting, Inc.

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Remote

Contract

Immediate need for a talented Clinical Documentation Coordinator CDI . This is a 06+months contract opportunity with long-term potential and is located in California(REMOTE ). Please review the job description below and contact me ASAP if you are interested. Job ID: 25-58162 Pay Range: $45 - $55/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Requirements and Technology Experi