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Lead and oversee the vendor in data management activities including database build, data review, and database lock, following requirements defined in the clinical protocol and in alignment with industry best practice guidelines and Caribou Clinical Development data standards and processes.
Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Strong knowledge with CDISC (CDASH/SDTM), medical dictionary coding standards, FDA and ICH guidelines, GCP, 21 CFR Part 11, Good Clinical Data Management Practices (GCDMP) Ability to development/oversee Data Management specific documentation including but not limited to the eCRF specifications, eCRF completion guidelines, edit check specifications, validation documents, DMP and DRP (Data Review Plan.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Syndicated Data experience: Experience with IRI, Nielsen, and other relevant platforms preferred. The Company is one of North America’s leading sales and marketing agencies specializing in outsourced sales, merchandising, category management and marketing services to manufacturers, suppliers and producers of food products and consumer packaged goods.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Reporting to the Sr. Director, Data Management, the Director, Data Management is responsible for the oversite of Data Management vendors to ensure timelines and deliverables are met and is accountable for all aspects of the clinical trial data management process from study start up through database lock, including escalations of issues when necessary.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Lead data management for clinical trials from launch to closeout. Proficiency in Medidata Rave or similar tools. Manage data collection, review, and reporting. Coordinate with vendors and senior management.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Familiarity with common software and technologies used in clinical data science (e.g., SAS, R, Python, Rave, Veeva). Represent Data Management, building strong relationships with Clinical Operations, Clinical Science, Biostatistics, Statistical Programming, Regulatory and IT teams.
$224,000 - $233,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Skilled in the use of data management software application, Medidata RAVE. Oversee, develop and maintain study-specific documentation, including Data Management Plans, eCRF specifications, CRF Completion Guidelines, Data Validation Guidelines, Data Transfer Specifications, Coding Guidelines, Post Production Database Change Control Documentation, Database Audit and Lock Procedures.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Prior experience in clinical research coordination or clinical research data management, and SignalPath, Complion, RedCap, Inform, Medidata RAVE, etc. Under general supervision of the Clinical Research Manager, the Clinical Research Professional provides data management support and assistance to theUniversity of Cincinnati Cancer Center Clinical Trials Office.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Innova Solutions Client is immediately hiring for a Manager/Sr Manager, Data Management. Conduct data management training as well as study specific training for the CDM and study teams.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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8 years of clinical data management experience in the clinical research industry with solid expertise in CDM operations and analytics; and. This includes SOPs for the development of Data Management Plans (DMPs), electronic Case Report Forms (eCRFs), Data Validation Plans (DVPs), eCRF completion guidelines and Data Review Plans (DRPs.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Design and develop data capturing tools: Electronic Data Capture (EDC) Systems (Eg: iMedidata Rave and IBM Clinical) eCOA, IRT; Manage electronic Trial Master File (eTMF) QC review eg: Veeva Vault; Lead the Audit and Inspection/Submission Readiness activities like documentation of QC and preparing Storyboards (Eg: FDA/EMA Submissions.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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SAS, Programmer, statistics, CDISC, SDTM, ADaM, CRO, clinical research, pharmaceutical, biotechnology, clinical data, data management, EDC, Electronic Data Capture, Medidata, Rave, Oracle, Inform, datasets, TLF, tables, listings, figures, programming, benefits, medical, dental, vision, 401k, Remote.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Familiarity with Medidata RAVE and/or other clinical data management software preferred. Review and manage key documents such as data management plans, guidelines for CRF completion, data review, SAE reconciliation, Vendor Oversight, TMF plans, and data audits.
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The app has 4.9 stars, garnering rave reviews from people who call it “life-changing” and their “#1 recommendation to parents”. Communicating and collaborating with cross-functional teams to understand requirements, design solutions, and deliver life-changing productsWeb, Android, and iOS hybrid application design, development, testing, and deploymentCloud infrastructure design, development, and managementBackend design and development including data structures and managementRunning sprint planning and executionOverseeing engineers during project executionRequirements.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Knowledge of GCP, CDISC, FDA, and ICH guidelines. Familiarity with Spotfire or other programming tools. A relocation package can be offered. Experience with EDC vendors and processes. 5+ years in pharmaceutical/biotech roles managing multiple trials.
ExpandApply NowActive JobUpdated 4 days ago
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