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You have a strong knowledge and practical experiences with high density data types in a clinical setting (genomics, transcriptomics, proteomics, flow cytometry, TCR sequencing, immune assays, etc.
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Master’s degree from an accredited university in fields such as outcomes research, epidemiology, biostatistics, data science, predictive analytics with 3 years relevant work experience is required; a doctoral degree (PhD, DrPH, ScD) is preferred.
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Build reports leveraging the Hyland Report Services module and/or writing custom SQL scripts against the OnBase Oracle database for support and administration purposes. Develop interfaces between OnBase and other applications using Hylands Unity toolkit, external database links, and/or custom integration applications to link enterprise applications with OnBase solutions, achieving a seamless user experience.
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Experience working with data management projects having experience in data analysis, data governance, data quality and lineage. Serves as an analytics resource to wider organization or business units, offering expertise on systems and data output.
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Thorough understanding of relational database components and experience in technical data management practices (validation plans, testing, and documentation) · Experience in CDISC conventions, i.e., CDASH, SDTM model and hands on experience implementing these models.
$60,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Broad knowledge of secondary pharmaceutical data sources such as Retail & Non-Retail data, Medical & Pharmacy Claims, EMR, Lab Test/Diagnostics, Chart Audits, Patient Hub & Specialty Pharmacy Data, 852/867 EDI and Health System/Payer – Plan hierarchies.
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This is a leadership position within MST that requires advanced technical expertise in protein purification skills, included but not limited to chromatography, filtration (tangential flow, depth, viral and dead end) in addition to general knowledge for mammalian cell culture processes and/or, formulation, protein product quality attributes, and advanced data analysis skills.
$157,100 - $217,100 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Senior Clinical Data Manager will be part of the cross-functional trial specific CTT and be responsible for core deliverables such as clinical database design/setup, data collection, data validation, manual review, and timelines.
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Langan is seeking an Environmental Engineer, Scientist, or Geologist to join its collaborative team in Princeton, NJ. This individual will serve a key function in providing site exploration activities including, but not limited to contaminated site investigation and remediation work; soil and groundwater sampling; vapor intrusion investigation; remedial investigation, design, implementation, and monitoring; pilot tests; data management, processing, and evaluation; and report preparation.
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Extensive knowledge of a broad array of systems including Clinical Trials Management System (CTMS); Risk Based Monitoring (RBM); Electronic Trial Master File (eTMF); Electronic Data Capture (EDC); Clinical Studies Operational Data Warehouse & Analytics; Site Training and Resource Management etc.
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Understanding of network infrastructure, database, cloud, data center operations, security. Stryten has developed a unique IoT driven, industry-specific, multi-tenant CRM for the industrial electric vehicle market and BESS. This is a chance to work with an embedded engineering team on one side that is working through the edge computing pieces of a multi asset system - battery, charger, vehicle, and gateway.
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Their responsibilities include: Installing, testing, troubleshooting, repairing or replacing cryptologic networks, physical security systems, electronic equipment, antennas, personal computers, auxiliary equipment, digital and optical interfaces, and data systems Configuring, monitoring and evaluating Information Operations (IO), Information Warfare (IW) systems and Information Assurance (IA) operations Cryptologic Technician Collection (CTR) - CTRs serve as experts in intercepting signals.
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Hands on experience in building metadata driven, reusable design patterns for data pipeline, orchestration, ingestion patterns (batch, real time); Experience in designing and implementation of solution on distributed computing and cloud services platform (but not limited to) - AWS, Azure, GCP; Utilize expertise in middleware technologies such as Mulesoft or Appian to design, develop, and deploy integration solutions.
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Proven experience with designing and conducting biomarker and genomics research experiments and reviewing and interpreting data to support drug development and improve clinical trial design. Initiates experimental design discussions based on existing gaps in clinical trial data and aids in development of biomarker and genomic research plans in collaboration with Bioanalysis, Genomics, and Biomarker Research department head, project teams, and external opinion leaders.
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Experience with general programming and data analysis tools/languages such as Python, R, MATLAB, Spotfire, etc., is required. knowledge and data to represent varying scales of drug pharmacology from target binding and modulation through disease pathophysiology and multi-drug pharmacology.
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