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Primarily responsible for the database design, setup, and maintenance of assigned clinical trials/projects in Medidata Rave. This role will also support our Systems team as administrative support for our standalone JReview system and assist with the implementation of a Genmab specific URL in Medidata Rave. Prior experience working in Medidata Rave in the core configuration environment or system implementation is preferred.
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Medidata, a Dassault Systèmes company, is leading the digital transformation of life sciences, creating hope for millions of people. As a game-changer in sustainable technology and innovation, Medidata, Dassault Systèmes company, is striving to build more inclusive and diverse teams across the globe.
ExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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Minimum of 1 year of experience in building case report forms (CRFs) using the Medidata Rave electronic data capture (EDC) system. The Medidata Rave Study Builder will be responsible for creating Rave studies for therapeutic oncology trials.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Develop, program, validate and maintain Medidata Rave EDC clinical trial databases according to company standards; Maintain and contribute to company library of standard Medidata Rave EDC CDASH compliant CRFs.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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MEDIDATA generates the evidence and insights to help pharmaceutical, biotech, medical device and diagnostics companies, and academic researchers accelerate value, minimize risk, and optimize outcomes.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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The ideal candidate will have in-depth experience in cell therapy, with specialized expertise in CAR-T therapy, solid tumors, leading a data management function, and expertise using Medidata Rave. This role encompasses the management of external Contract Research Organizations (CROs), acting as a Subject Matter Expert (SME) for all data management activities, and ensuring the highest data quality and integrity across the clinical operations organization.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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CTMS systems like CRIO, clinical conductor, Clinical Ink; EDC systems like MediData, Oracle, and Inform; ePRO, eConsent and IWRS/IXRS, etc. CTMS systems like CRIO, clinical conductor, Clinical Ink; EDC systems like MediData, Oracle, and Inform; ePRO, eConsent and IWRS/IXRS, etc.
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The Travel Clinical Research Coordinator will be mentored by their CRC Lead, Site Manager, Senior Manager, and other leaders within clinical operations. Based out of the San Antonio, TX area, The Travel Clinical Research Coordinator Based primary responsibilities are to utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
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Hands-on experience with at least one EDC system (e.g.: Medidata Rave, Inform, Veeva etc.,) 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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Product Marketing Director, Clinical Trial Financial Management, CTMS and eTMF Medidata: Powering Smarter Treatments and Healthier People Medidata, a Dassault Systèmes company, is leading the digital transformation of life sciences, creating hope for millions of people.
$135,000 - $180,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Understanding of industry standard technologies to support Clinical Development needs (e.g., CTMS, SAS, R or Python, Data Warehouses, SharePoint) Configure other modules within the EDC ecosystem such as coding, integration of IRT, safety system, local labs etc.
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We are seeking a Technical Lead/Architect with knowledge of SAS software and Medidata EDC. Understanding of the SAS Studio and Medidata EDC applications. Understanding of the Medidata EDC applications.
RemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Experience integrating other clinical trial modules (e.g.: lab, safety, IRT, coding etc.,) with the EDC system. Prepare, test and implement post production changes as per study needs while ensuring data integrity.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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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. Create eCRF specifications, design, develop and validate clinical trial setup in EDC.
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U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. This position is currently classified as “remote” in accordance with Takeda’s Hybrid and Remote Work policy.
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