director, Clinical data management Jobs

41 - 60 of 242 Jobs

Clinical Supply Chain SpecialistJob Title - Clinical Supply Chain Specialist

NexInfo Solutions, Inc.Company Name - NexInfo Solutions, Inc.

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Foster City, California, USA

Contract, Third Party

About Nexinfo: NexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors. They offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions. The company aims to help businesses across industries achieve their goals through industry best practices, lean process design, and advanced software solutions. Their ERP-related services address challenges

Eyecare Clinical Systems EngineerJob Title - Eyecare Clinical Systems Engineer

Sunrise Systems, Inc.Company Name - Sunrise Systems, Inc.

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Remote

Contract

Our client, a leading vision care insurance company, is looking for an Eyecare Clinical Systems Engineer. This is for an initial duration of 5 months and is fully remote. Must Haves: This person will work with Ventures teams to understand clinical hardware at the sites, installation and configuration of equipment.Must have clinical experience in Eyecare and eye equipment (eye exam)Need to have Clinical Application function with clinical devices.Must understand data traffic.Able to configure and

Clinical Research EngineerJob Title - Clinical Research Engineer

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 Clinical Research Engineer to join its innovative team focused on advancing digital health technologies. In this role, you will collaborate closely with clinical scientists and cross-functional teams to design, execute, and monitor clinical studies, with a focus on biosensor data quality and analysis. The ideal candidate will have experience with clinical datasets, wearable health sensors, cloud data solutions like AWS, and familiarity with regulatory sta

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 SME Project Manager -AI/Gen AI knowledgeJob Title - Clinical SME Project Manager -AI/Gen AI knowledge

Apex 2000Company Name - Apex 2000

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New York, New York, USA

Contract

Clinical SME Project Manager -AI/Gen AI knowledge Location: New York Duration: 9-12 month JD: Total Yrs. of Experience 10+ Relevant Yrs. of experience 10+ Mandatory skills Clinical R&D + Project management Comfortable working in a matrix environment with clinical, regulatory, and tech teams.Demonstrates strong problem-solving and decision-making under tight timelines.Ability to lead and coordinate cross-functional teams from offshore and onshore.Strong stakeholder management and communication

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

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.

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 Business Systems Analyst - D/T NYC, onsiteJob Title - Clinical Business Systems Analyst - D/T NYC, onsite

Winston Staffing ServiceCompany Name - Winston Staffing Service

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New York, New York, USA

Contract

A clinical business analyst plays a crucial role in healthcare organizations by analyzing clinical data and operations to improve business performance and ensure regulatory compliance. Duties & Responsibilities Analyze and document business requirements and processes; communicate requirements to technical personnel through the construction of basic conceptual data, process models and flowcharts, and technical specifications.Interview end users, stakeholders, and project sponsors in order to ass

Clinical Systems Analyst TrizettoJob Title - Clinical Systems Analyst Trizetto

Tech Pro Inc.Company Name - Tech Pro Inc.

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Remote

Contract

send your resume directly to my email kumar @ techpro-inc . com with Subject: Applying from Dice (only this line) OR click on Apply now Job Description: Configuration Management and Content Specialist Configuration Management Documentation: Create comprehensive documentation of configuration management processes. Develop process flowcharts for configuration management. Write step-by-step setup and testing procedures. Prepare troubleshooting guides for common issues. Document version control a

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Bridgewater, New Jersey, USA

Full-time

Responsibilities: Lead and participate in the development and validation of high quality CDISC datasets based on the implementation guides and consultations with sponsors, project leads, systems analysts, other programmers, and end users. Use your expertise in data standards and regulatory requirements to lead discussions with clients about appropriate approaches to database design. Use study protocol, CRF, Data Transfer Agreements from vendors, data sources, CDISC CT, TAUGS, and CDISC implement

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

SanofiCompany Name - Sanofi

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Morristown, New Jersey, 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

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

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 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

Digital Biomarker Innovation Clinical LeadJob Title - Digital Biomarker Innovation Clinical Lead

SanofiCompany Name - Sanofi

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Morristown, New Jersey, USA

Full-time

Job DescriptionAbout 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 Clinical Innovation team at Sanofi is responsible for identifying, accelerating, and scaling innovations that can serve to improve operations and/or outcomes for patients, sites, and sponsors of clinical trials. The Clinical Innovation tea

Clinical Services Project ManagerJob Title - Clinical Services Project Manager

Software Guidance & AssistanceCompany Name - Software Guidance & Assistance

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Tucson, Arizona, USA

Contract

Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Services Project Manager for a contract assignment with one of our premier Pharmaceutical clients in Tucson, AZ. Responsibilities : Manages multiple clinical and lab services projects of less complex nature from initiation through contract completion. Applies project management skills and experience in delivering projects on time, within budget and with high customer satisfaction. Facilitates cross-functional interacti

Integration Engineer SrJob Title - Integration Engineer Sr

University Of UtahCompany Name - University Of Utah

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Salt Lake City, Utah, USA

Full-time

Announcement Details Open Date 06/24/2025 Requisition Number PRN42287B Job Title Integration Engineer Sr Working Title Integration Engineer Sr Job Grade G FLSA Code Computer Employee Patient Sensitive Job Code? No Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary Arranged with the Supervisor VP Area U of U Health - Academics Department 01271 - Biomed Informatics Core CCTS Location Campus City Salt Lake City, UT Type of Recruitment Extern

Clinical Supply Systems AdministratorJob Title - Clinical Supply Systems Administrator

Johnson & JohnsonCompany Name - Johnson & Johnson

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Remote or Horsham, 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

R&D Engineer II (Clinical Engineering)Job Title - R&D Engineer II (Clinical Engineering)

Johnson & JohnsonCompany Name - Johnson & Johnson

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Santa Clara, California, USA

Full-time

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