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The IRT provides support for 17 adult, Medical/Surgical, inpatient nursing units at Iowa Methodist Medical Center, Iowa Lutheran Hospital, and Methodist West Hospital. The Internal Resource Team (IRT) provides support and additional resources to nursing units throughout UnityPoint Health—Des Moines during times of vacancy, high acuity, and census variations.
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Generating the MTRs - Planners on IRT, folder to create the IQS MTRs, coordinate shipment.) Uploads of Clinical Supply Chain Documents file documents to the electronic Trial Master File (eTMF.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Experience in survey design and quantitative methods such as patient-reported outcome measurement development (e.g., Classic Test Theory and IRT knowledge) and/or patient preference studies (trade-off methods and DCE.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Interactive Response Technology (IRT)/Interactive Web Response Systems (IWRS) and data warehouse technologies as applied to clinical trials. Ensure archival of all Data Management Trial Master File (TMF) documents.
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Oversee vendors and actively participate in all UATs for vendor systems, including IRT, EDC, Central Labs, etc. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Bayer and Vertex Pharmaceuticals.
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Lead and oversee Electronic Data Capture (EDC) build, migration and deployment including creation and execution of user acceptance testing plans and test scripts, and implementation of data integrations with external vendor data sources (e.g., IRT, laboratory, imaging.
RemoteExpandApply NowActive JobUpdated 21 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.
Full-timeExpandApply NowActive JobUpdated 4 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: Master’s degree in Pharmaceutical Sciences, Pharmacology or Toxicology or related field or foreign academic equivalent plus 6 years of related experience.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experience programming with clinical data within pharmaceutical and/or biotechnology companies, clinical IRT/eCOA systems, or EDC. Experience with any data analysis package such as SPSS, SAS, R, or MATLAB.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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More About Us : Independence Realty Trust, Inc (NYSE: IRT) is a real estate investment trust that owns and operates Class A and Class B multifamily apartments. This Evergreen Requisition is an advertisement for positions that IRT Living hires for throughout the year.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Configure other modules within the EDC ecosystem such as coding, integration of IRT, safety system, local labs etc., Experience integrating other clinical trial modules (e.g.: lab, safety, IRT, coding etc.,) with the EDC system.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Lead the development, review and User Acceptance Testing (UAT) of the Interactive Response Technology (IRT) system. Utilize appropriate software and IT systems (e.g. IRT, MS Office, MS Project, Smartsheets, and others) to effectively manage key project activities.
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Manage the deployment of Suvoda IRT systems into all environments, completing all required documentation. Work within a cross-functional project team to develop Interactive Response Technology (IRT) for randomization and drug supply management.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The (Senior) Clinical Trial Manager is accountable for delivery of selected and/or regional activities within a trial (e.g., manage and oversee vendor deliverables, collaborate with functions to set up activities [e.g., DM, IRT, and eRT], support site activation and recruitment, support data review/cleaning activities, support PI/ICF development.
$95,625 - $159,375 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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At least 5 years, additional work experience directly related to the duties of the job and/or completed higher education; preferred PharmD with health outcomes research, PhD in pharmaceutical sciences, epidemiology, health outcomes, or psychology (specifically, social psychology, behavioral science, experimental psychology.
ExpandApply NowActive JobUpdated 7 days ago
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