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Experience with clinical trial databases (e.g., Medidata Rave, Veeva, etc. As a CTM, you will be responsible for planning and managing our early development clinical trials in kidney disease while ensuring high quality data and timely clinical trial conduct per GCP standards.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Serve as system administrator to grant user access using iMedidata Cloud Administration for RAVE EDC, Coder, Lab Admin, RTSM and MMI (Imaging) provide Oversight, guidance, and design of study build activities on Rave URL.
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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 4 days ago - UpvoteDownvoteShare Job
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Ability to work with spreadsheets (such as Excel), familiarity with databases (ex: Medidata, RAVE, IRIS, NSABP, GOG, RTOG etc.) In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and data entry for research protocols, databases and projects within Hartford Healthcare Cancer Institute, and ensures the data quality and integrity for each clinical trial.
ExpandApply NowActive JobUpdated 3 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, Define.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Experience with clinical trial databases (e.g., Medidata Rave, InForm, etc. Develop and review informed consent forms, case report forms, study manuals, and other clinical trial materials.
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Hands-on experience with at least one EDC system (e.g.: Medidata Rave, Inform, Veeva etc.,) Confirm archival and inspection readiness of all Clinical Technology Trial Master File (TMF) documents.
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Clients rave about us, attorneys trust us and insurance companies fear us. We are a trial personal injury law firm that approaches clients and team members differently. Ability to manage your caseload to include written discovery, depositions, motions, briefing, and taking cases to trial as a member of our trial team.
Full-timeExpandApply NowActive JobUpdated 18 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.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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In collaboration with internal/external experts on biostatistics, clinical pharmacology, translational medicine, clinical operations and data management, contributes to the development of the plans to execute on trial design including CRF design, data review plan, statistical analysis plan review and finalization.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Experience integrating other clinical trial modules (e.g.: lab, safety, IRT, coding etc.,) with the EDC system. The EDC Engineer will work with Data Management and Standards teams to implement new processes as well as enhance existing processes for efficiencies and compliance with Takeda Clinical trial builds.
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Proficiency with Clinical Trial Management Systems (CTMS), RAVE and Veeva Vault systems preferred. Proficiency with Clinical Trial Management Systems (CTMS), RAVE and Veeva Vault systems preferred.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Takeda Development Center Americas, Inc. is seeking a Senior Manager, Clinical Data Management in Lexington, MA with the following requirements: Masters degree in Pharmaceutical Sciences, Pharmacology or Toxicology or related field or foreign academic equivalent plus 6 years of related experience.
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Robust experience with core data management activities, EDC (eg, Medidata Rave) and use of Data Review tools. 5+ years as a Trial Data Manager with full accountability across study start-up, conduct, and lock.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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This consultant will also be responsible for then reporting within EDC systems such as VeevaVault and Medidata Rave. Medidata Rave & VeevaVault Familiarity. This consultant will also be responsible for then reporting within EDC systems such as VeevaVault and Medidata Rave.
ExpandApply NowActive JobUpdated 6 days ago
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