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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

Clinical EHR Project Manager (Hospital domain exp.)

Shift Code Analytics

Remote

Contract, Third Party

Hi, Hope you are doing well I have an urgent opening of Clinical EHR Project Manager at remote role Position Type: Contract Location: Remote, United States Onsite Flexibility: 100% Remote Description: Interview : Video Description : Our client is seeking an EHR Project Manager with experience integrating 3rd party applications. Epic experience is not required but EHR is required. Regards, Nitin Gupta Team Lead-Recruitment ShiftCode Analytics Inc., 5118 Sylvester loop Tampa, Florida 33610 Direc

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

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

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

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

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 Development Scientist

ComTec Information Systems

Bothell, Washington, USA

Contract

Clinical Development Scientist Hybrid role. 3 days/week in office Bothell WA/Cambridge MA/ Plymouth MN 12 Months Ultrasound, Senior Clinical Development Scientist The Senior Clinical Development Scientist for the Ultrasound group will be responsible for developing, generating, and disseminating clinical and economic evidence ensuring innovation, and transformation with best-in-class clinical evidence. Your role: Contribute strategic guidance for clinical and economic evidence related to the en

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

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 Business Operations Associate

Informatic Technologies

Remote

Contract

One of our leading Pharmaceutical client is looking to hire a Clinical Business Operations Associate in Morristown, NJ. Position Summary: The role of the Clinical Business Operations Associate is to review and approve invoices and expenses against contracts established with the Research and Development function of Clinical Operations globally. Additionally, support and manage a variety of clinical contracts, various contract administrative and legal matters as needed. This role can work from Cli

Clinical Lead, I&I

Sanofi

Cambridge, Massachusetts, USA

Full-time

Job Title: Clinical Lead, I&I Location: Cambridge, MA or 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 Clinical Lead is the primary clinical lead for a clinical development program, reporting into the Global Project Head (GPH), and leading a team of Clinical Research Directors and C

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

Director 2, Clinical Engineering - G

Next Step Systems

Zanesville, Ohio, USA

Full-time

Director 2, Clinical Engineering We are seeking an experienced individual for a Director 2, Clinical Engineering opening in Zanesville, OH. The Director 2, Clinical Engineering will oversee numerous types of medical equipment, offer hands-on experience, and provide leadership and process-improvement knowledge to staff. The Director 2, Clinical Engineering should be a high-level leader that can manage a team of supervisors and technical professionals. This is a fantastic opportunity for any acco

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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

Clinical Resource Analyst - PRN

Mat-Su Medical Group

Palmer, Alaska, USA

Part-time

Job Summary The Clinical Resource Analyst provides support to physicians and staff for certified clinical system(s). Participates in implementation and upgrade of Electronic Health Records (EHR) applications and interfaces. Acts as clinical liaison between corporate IT, hospital leadership and clinical end users. Clinical System/Resource Analyst plays a vital role in healthcare organizations by ensuring that clinical information systems EHRs, Laboratory Information Systems (LIS), and Radiology I

QA Clinical Supplies Specialist

Zachary Piper Solutions, LLC

Lansdale, Pennsylvania, USA

Full-time

Piper Companies is seeking a QA Clinical Supplies Specialist to join a major pharmaceutical manufacturing company located in Lansdale, PA. This is a Hybrid role. The QA Clinical Supplies Specialist will ensure the quality, compliance and integrity of clinical trial supplies. Responsibilities of the QA Clinical Supplies Specialist include: Ensure clinical supply materials meet company policies and regulatory standards. Lead projects aimed at improving process performance, including yiel

IT Product Manager - Clinical Systems

Eli Lilly and Company

Indianapolis, Indiana, USA

Full-time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

Associate Project Manager, Office for Global Clinical Operations

Mitchell Martin, Inc.

Sacramento, California, USA

Full-time, Contract

Title: Associate Project Manager, Office for Global Clinical OperationsLocation: Remote Employment Type: ContractCompensation: Pay Range: $46.55-$66.50 Per HRDescription: Lead data consolidation and analytics for specific deliverables. Implement and review data analyses for accuracy and nuances. Oversee process documentation and implementation. Develop reports and track department metrics. Monitor metrics to identify risks and set goals. Support proposal formulation for business solutions. Prepa