junior clinical analyst Jobs

41 - 60 of 130 Jobs

Clinical Research AssociateJob Title - Clinical Research Associate

OSI Engineering, Inc.Company Name - OSI Engineering, Inc.

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Mountain View, California, USA

Full-time

A global device company is looking for a motivated Clinical Research Associate to support studies involving wearable sensor technology and human subject data collection. Key responsibilities include executing data-collection protocols, preparing devices, coordinating study logistics, and ensuring high-quality data. If you have a background in engineering or a related field, experience with mobile sensors or wearables, and a passion for advancing health technology, we invite you to apply and joi

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

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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Boulder, Colorado, USA

Full-time

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

Clinical Data managerJob Title - Clinical Data manager

Intone Networks Inc.Company Name - Intone Networks Inc.

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Remote

Contract, Third Party

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

Bidirectional Clinical Data Exchange ArchitectJob Title - Bidirectional Clinical Data Exchange Architect

Digital Minds Technologies Inc.Company Name - Digital Minds Technologies Inc.

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Remote

Contract

Job Title: Bidirectional Clinical Data Exchange Architect Location: Durham, NC (Remote) Project Duration: 6+ Months Contract (Only W2 Contracts) Job Description: The Bidirectional Clinical Data Exchange Architect will be responsible for designing, implementing, and maintaining bidirectional clinical data exchange solutions. This role requires a deep understanding of healthcare interoperability, data exchange standards, and clinical workflows. Key Responsibilities: Architecture Design: Design and

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 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

Clinical Lead, Early Clinical and Experimental TherapeuticsJob Title - Clinical Lead, Early Clinical and Experimental Therapeutics

SanofiCompany Name - Sanofi

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Cambridge, Massachusetts, USA

Full-time

Job DescriptionJob Title: Clinical Lead, Early Clinical and Experimental Therapeutics Location: Cambridge, MA Morristown, NJ About the Job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress. Join our state-of-the-art ECET department as a Clinical Lead, ECET and you ll drive the translation between preclinical development t

Clinical Lead, Early Clinical and Experimental TherapeuticsJob Title - Clinical Lead, Early Clinical and Experimental Therapeutics

SanofiCompany Name - Sanofi

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Morristown, New Jersey, USA

Full-time

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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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.

Senior Clinical Outcomes Assessment (COA) LeadJob Title - Senior Clinical Outcomes Assessment (COA) Lead

SanofiCompany Name - Sanofi

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Cambridge, Massachusetts, USA

Full-time

Job Title: Senior Clinical Outcomes Assessment (COA) Lead Location: Cambridge, MA, Morristown, NJ About the Job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress. The remit of the Clinical Outcome Assessment (COA) team at Sanofi is to incorporate the patients' perspective (and other subjective perspectives) into clinica