entry level clinical data manager Jobs

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Clinical Research Associate I, Tan Lab

CEDARS-SINAI

Los Angeles, California, USA

Full-time

Job Description The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study

Clinical Systems Specialist

Tandym Tech

Woburn, Massachusetts, USA

Contract

A biotech company in Massachusetts has a great Remote contract opportunity awaiting a new Clinical Systems Specialist. In this role, the Clinical Systems Specialist will be responsible for supporting the lifecycle management of clinical systems for Global Development Operations. To be considered for this opportunity, the qualified professional must be able to work on a W2 basis. Responsibilities: Work on planning, design, configuration, and deployment of new clinical systems and enhancements

Senior Clinical Java Architect

Tror

Eden Prairie, Minnesota, USA

Contract, Third Party

Position: Senior Clinical Java Architect Location: Eden Prairie, Minnesota (Hybrid 3 days onsite) Duration: 6+ months Contract: C2C/w2 Job Description: Seeking a highly experienced Clinical Java Architect with a strong background in designing and implementing complex, high-availability clinical systems in healthcare settings. This role demands deep expertise in Java-based backend architectures, along with hands-on knowledge of healthcare data standards (e.g., HL7, FHIR, CCD, DICOM) and int

Clinical Project Manager

Info Way Solutions

New York, New York, USA

Third Party, Contract

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 across time zones and geographies.Proactively identify opportunities for process automationSkilled at translating business needs into technical project requirements.Ability t

Clinical Supply Chain Specialist

NexInfo Solutions, Inc.

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

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 Research Associate I - Butte Lab - Department of Neurosurgery (Per Diem)

CEDARS-SINAI

Los Angeles, California, USA

Full-time

Job Description When the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. We invite you to consider this phenomenal opportunity! Dr. Pramod Butte, Ph.D. is looking for a Clinical Research Associate I to join a diverse team! The primary focus of the Butte Laboratory is translational research in the field of bio-photonics. The But

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

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

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

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

SAP DTS Lead - Intelligent Clinical Supply Management (ICSM) - Remote- CTC

Care IT Services Inc

Remote

Contract

Job Description: The DTS Lead ICSM is responsible for leading the design, implementation, and optimization of SAP s Intelligent Clinical Supply Management (ICSM) solution. This role supports clinical trial operations by ensuring efficient planning, forecasting, packaging, labeling, and distribution of clinical trial materials across global sites, while maintaining regulatory compliance and end-to-end visibility. Responsibilities: Solution Design & Implementation: Lead the deployment of SAP ICSM

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 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 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