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The Sr. Clinical Data Manager will be responsible to support all aspects of data management from study start-up to database lock including EDC design, data review/cleaning, query management, data reconciliation, and data transfer specifications.
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Experience working with an Electronic Data Capture system (EDC) (e.g. Medidata Rave) and with other databases (e.g. Central Imaging, IVRS/IWRS) Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
$150,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Experience using Medidata EDC and data visualization programs (e.g., R-Shiny, SAS, SpotFire, Tableu, Excel Pivot Tables, etc.) Experience using Medidata EDC and data visualization programs (e.g., R-Shiny, SAS, SpotFire, Tableu, Excel Pivot Tables, etc.
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In-depth knowledge of clinical trial process, EDC systems (i.e., Medidata Rave, InForm, etc.) Manages and oversees reconciliation between EDC and non-EDC database, such as, SAE, Lab, and biomarker.
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The Explosive Detection Canine Handler partners with a trained Explosive Detection Canine (EDC) to conduct searches in/at assigned client sites, including corporate buildings, loading docks, delivery vehicles, open areas and/or other situations as needed.
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Lead the development of EDC data review listings, SAS clinical programming report specifications and data visualization outputs. Lead and oversee Electronic Data Capture (EDC) build, modifications and deployment including creation and execution of User Acceptance Testing (UAT) plans and test scripts, and implementation of data integrations with external vendor data sources (e.g., IRT, laboratory, Imaging.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Participates in assigned activities related to user acceptance testing (UAT) of clinical systems, including EDC and interactive response technology (IRT) and may contribute to the authoring of systems requirements.
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Ensures the quality of clinical data within the EDC and other databases through data review and data reconciliation processes and communicates any outstanding issues. ResponsibilitiesIndependently leads EDC development, including CRF development, EDC specification process, edit check development and User Acceptance Testing including test scripts and execution logs, issue logs, and UAT summary reports.
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Works with other functions to complete set up of EDC and other study data collection tools such as IRT, ePRO. Ensure archival and inspection readiness of all Data Management Trial Master File (TMF) documents.
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Conduct Clinical Research Coordinator activities for assigned clinical research device studies including consenting participants, conducting study sessions, maintaining device accountability, and completing data entry into the Electronic Data Capture (EDC) system.
ExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Proficient with Microsoft applications (Word, Excel, PowerPoint, and Outlook) other 3rd party EDC/EMR applications. The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI), Manager of Compliance and Contracts, and the Administrative Nurse II.
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Desired Skills: Experience with clinical databases i.e. EDC and EHR systems. Fluency in CDISC, MedDRA and other health data standards. Job Description: As a Clinical Data Manager/Analyst in the Quantitative Sciences organization, you will be responsible for supporting and managing the collection, capture, quality, and integrity of data, from diverse sources, including electronic health records, eCRF, ePRO, digital health technologies including apps and sensors, digital biomarkers, advanced specialty labs, images, and others.
$82 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Strong knowledge and experience in EDC and other key technologies (e.g., IXRS, data visualization) Participate in the development of EDC custom report specifications, SAS Clinical Programming report specifications and/or associated outputs as needed.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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We offer various project engagement models – Onsite/Onshore, Offshore, Hybrid (Onsite + Offshore) and EDC (Extended Development Center). EDC offers enhanced level of engagement facilitating strategic partnership with the clients by setting up center which leverages our processes, infrastructure and operational capabilities.
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Experience with EDC systems (e.g., Medidata Rave, Oracle Clinical) and other clinical trial data management tools. Experience with EDC systems (e.g., Medidata Rave, Oracle Clinical) and other clinical trial data management tools.
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edc job in South San Francisco, CA
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