Clinical Data Manager Jobs

Refine Results
21 - 40 of 111 Jobs

Clinical Research Coordinator - (Exercise Physiology/Kinesiology/Nutrition) - Onsite

VIVA USA INC

•

Valhalla, New York, USA

Contract

Title: Clinical Research Coordinator - (Exercise Physiology/Kinesiology/Nutrition) - Onsite Mandatory skills: clinical research, good clinical practice, Google Cloud Platform, human physiology, laboratory-based clinical research strategy, research hub, study coordination, clinical trial document management, subject recruitment, screening, scheduling, data collection, data entry, writing, research projects Description: Additionally, the specific job responsibilities of the incumbent are as foll
Easy Apply
Posted 1 day ago

Clinical Research Coordinator

Zachary Piper Solutions, LLC

•

Raleigh, North Carolina, USA

Full-time

Piper Companies is seeking a highly organized and proactive Clinical Research Coordinator (CRC) to support clinical trials across multiple therapeutic areas on-site in the Raleigh, NC area. This role is essential in ensuring smooth trial execution within a clinical site network, with a focus on phlebotomy and patient coordination. Key Responsibilities of the Clinical Research Coordinator: Oversee day-to-day clinical trial activities while ensuring compliance with Google Cloud Platform, IRB, and
Posted 11 days ago | Updated 8 days ago

Clinical Research Coordinator

Zachary Piper Solutions, LLC

•

Raleigh, North Carolina, USA

Full-time

Piper Companies is seeking a detail-oriented and proactive Clinical Research Coordinator (CRC) to join our growing clinical research team. The ideal candidate will have hands-on phlebotomy experience and a strong background working within a clinical site network environment. This role is essential in supporting the execution of clinical trials across multiple therapeutic areas. Responsibilities for the Clinical Research Coordinator: Coordinate and manage day-to-day clinical trial activities in
Posted 19 days ago | Updated 8 days ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Lake Success, New York, 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
Posted 2 days ago | Updated 11 hours ago

Bidirectional Clinical Data Exchange Architect

Digital Minds Technologies Inc.

•

Remote

Contract

Job Title: Bidirectional Clinical Data Exchange Architect Location: Durham, NC (Remote) Duration: Long term contract 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 develop architecture for bidi
Easy Apply
Posted 35 days ago | Updated 29 days ago

Clinical Development Scientist

Daddy Recruiter LLP

•

Bothell, Washington, USA

Contract

Job Title - Clinical Development Scientist; This is a hybrid role. 3 days/week in office (bothell or cambridge locations). I am open to candidates in Plymouth (MN) as well. Notes from the manager: I need a PHD or MD candidate who has a scientist background - This is a requirement. I need someone who has worked in the medical device space who has designed studies for regulatory environments. Reporting protocols experience within this industry also required. US Regulations experience is required
Easy Apply
Posted 15 days ago

Sr. eCOA (Electronic Clinical Outcome Assessment) Project Manager

EA Team, Inc.

•

Remote

Contract

Role : Sr. Sr. eCOA (electronic Clinical Outcome Assessment) Project Manager with strong experience in eClinical suite implementation Location : Remote Duration : Long Term Contract Role Overview: The PM will lead the planning, execution, and delivery of projects involving eClinical technologies, with a strong emphasis on eCOA (electronic Clinical Outcome Assessment) systems. This includes managing cross-functional teams, aligning with regulatory and compliance standards, and ensuring timely
Easy Apply
Posted 9 hours ago

SAS Clinical Trails Programmer

Katalyst Healthcares and Lifesciences

•

Cary, North Carolina, USA

Full-time

Responsibilities: The consultant will provide programming/analytical support utilizing client as the primary programming language to create and manage the production of analysis reports. summary tables/listings and graphs for clinical trials submitted to various regulatory bodies worldwide. The consultant must have excellent communication skills and must be able to communicate about the techniques developed and results of analysis both to executives and other analysts in the organization. Pe
Posted 42 days ago | Updated 11 hours ago

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
Posted 42 days ago | Updated 11 hours ago

Clinical QA Lead

Bahwan CyberTek Inc.

•

Boston, Massachusetts, USA

Third Party, Contract

Title : Clinical QA Lead Location: Boston, MA (Hybrid) Duration : Long term Description: Minimum of 8 years of software quality testing experience and 12+ years IT/Industry experience. 5+ years of experience in Computer Systems Validation (CSV) in the context of Good Clinical/Manufacturing Practices (GxP) is preferred. Experience with software application test planning and functional testing, performance testing, developer management, and defect management using Application lifecycle management
Easy Apply
Posted 14 days ago

Project Manager Clinical Programs

Triune Infomatics Inc

•

Martinez, California, USA

Contract

Role: Project Manager Clinical Programs Location: Martinez, CA (3 days onsite) Duration: 6 Months Contract to Hire Summary: The Client is seeking a Project Manager for projects that support clinical programs including Quality Incentive Program (QIP), Provider Documentation, and Hierarchical Condition Category (HCC) coding initiatives. QIP is a statewide performance-based payment program that enables public healthcare systems to earn incentive payments by improving quality and demonstrating pe
Easy Apply
Posted 2 days ago | Updated 14 hours ago

Solution Architect - Clinical Imaging

Randstad Digital

•

Remote or Warren, Michigan, USA

Contract

job summary: We have a 12 month contract opportunity for a Solution Architect - Clinical Imaging. This role is fully remote but must work CST business hours. Experience Required: 8+ years Job Summary: We are seeking a highly skilled Solution Architect with extensive experience in clinical imaging technologies, specifically in radiology and cardiology. The ideal candidate will be responsible for creating high-level designs, understanding dependencies, configurations, and installation requirem
Posted 7 days ago | Updated 2 hours ago

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
Posted 42 days ago | Updated 11 hours ago

IT - Clinical Informaticist ? Product Development

NTT DATA Americas, Inc

•

Remote or St. Louis, Missouri, USA

Contract

At NTT DATA, we know that with the right people on board, anything is possible. The quality, integrity, and commitment of our employees have been key factors in our company s growth and market presence. By hiring the best people and helping them grow both professionally and personally, we ensure a bright future for NTT DATA and for the people who work here. For more than 25 years, NTT DATA have focused on impacting the core of your business operations with industry-leading outsourcing services a
Easy Apply
Posted 18 hours ago | Updated 6 hours ago

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
Posted 29 days ago | Updated 11 hours ago

Clinical Informatics Support Analyst

Futrend Technology

•

Bethesda, Maryland, USA

Full-time

Futrend Technology has an opening for a Clinical Informatics Support Analyst to join our team of professionals in support of one of our customers in a Clinical Health Care environment. About Futrend: Futrend Technology, Inc. is a business and technology solutions provider. Our primary focus and core competencies are in Healthcare IT and program support. We excel at providing customers with high-value solutions that support their missions and meet their most critical objectives and business need
Easy Apply
Posted 23 days ago | Updated 1 day ago

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
Posted 42 days ago | Updated 11 hours ago

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
Easy Apply
Posted 28 days ago | Updated 17 hours ago

Epic Ancillary Clinical Application Analyst

Apidel Technologies

•

Newport Beach, California, USA

Contract

Job Title: Ancillary Clinical Application Analyst Working Hours: 7 AM-5 PM Location: Newport Beach, CA 92663 Duration: 06- Contract Months [Potential for Extension based on performance and project needs] Top Skills: Certifications in EPIC and third-party apps are not important; the manager wants to see candidates with knowledge of integrations with EPIC and third-party apps.We will be focused on backend implementation and testing, and we must be strong.Job Description: The Applications Analyst
Easy Apply
Posted 37 days ago | Updated 19 days ago

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
Posted 40 days ago | Updated 11 hours ago