Entry Level Clinical Data Manager Jobs

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Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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

Eyecare Clinical Systems Engineer

Sunrise Systems, Inc.

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 Engineer

OSI Engineering, Inc.

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 Associate

OSI Engineering, Inc.

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 knowledge

Apex 2000

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

Computer System Validation Analyst - R Studio & Clinical Systems

Katalyst Healthcares and Lifesciences

Remote or New Jersey, USA

Full-time

Responsibilities: Lead validation planning, risk assessment, and execution for R Studio, GitLab, and Medidata Rave EDC. Develop and execute validation documentation including: Validation Plans (VP.). User Requirements Specifications (URS.). Risk Assessments (RA.). Functional and Design Specifications. Traceability Matrix (RTM.). Test Protocols (IQ/OQ/PQ or CSA-based scripts.). Validation Summary Reports (VSR.). Collaborate with cross-functional stakeholders including Clinical Data Mana

Bidirectional Clinical Data Exchange Architect

Digital Minds Technologies Inc.

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

Sr. Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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 Programmer

Katalyst Healthcares and Lifesciences

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 Systems Analyst Trizetto

Tech Pro Inc.

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 Programmer

Katalyst Healthcares and Lifesciences

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

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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.

Clinical Field Service Engineer

Nityo Infotech Corporation

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 Research Associate

Zachary Piper Solutions, LLC

Sacramento, California, USA

Full-time

Piper Companies is currently seeking an Oncology Clinical Research Associate (CRA) for an opportunity in Sacramento, California (CA). The Oncology Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Oncology Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monito

Clinical Research Associate

Zachary Piper Solutions, LLC

Los Angeles, California, USA

Full-time

Piper Companies is currently seeking a Clinical Research Associate (CRA) for an opportunity in Los Angeles, California (CA). The Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monitoring and study activation

Clinical Editing Coding Analyst | Remote | Contract

Walker Healthforce

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, investig

Clinical Services Project Manager

Software Guidance & Assistance

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

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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

Clinical Supply Systems Administrator

Johnson & Johnson

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)

Johnson & Johnson

Santa Clara, California, 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