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Years of mainframe experience in IBM JCL, CA, JCL, and utilities, COBOL, REXX, EasyTrieve, VSAM, IDMS, Endevor, File Master, Dispatch, View, UniTech and Remedy utilities. years of mainframe experience in IBM JCL, CA, JCL, and utilities, COBOL, REXX, EasyTrieve, VSAM, IDMS, Endevor, File Master, Dispatch, View, UniTech and Remedy utilities.
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Proven experience as a Scrum Master and Business Analyst within the financial services industry, specifically with Loan IQ systems. We are looking for a seasoned Scrum Master/Business Analyst with extensive experience in Loan IQ to facilitate the delivery of complex projects.
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Experience and knowledge of Data Integration, Master Data Management, Data Quality, and Data Governance technologies are preferable. Experience with one or more e.g. AWS or Microsoft Azure, Snowflake, and Databricks.
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Minimum 4 years of relevant work experience in Pharmaceutical Manufacturing System Processes (GxP) Systems environment and related Master Data Management. Develop and implement robust site Governance around E2E ERP Master Data, including defining and authoring local standardizations, SOPs, and work instructions.
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Set-up, organize, and maintain clinical study documentation (e.g. Trial Master File documents, clinical study site documents, email correspondence, training materials, etc.) Pharming is seeking to hire a Clinical Trial Assistant (CTA) to bring general administrative support to the Clinical Operations Department and assistance to Project Manager(s), Clinical Project Coordinator(s) and Department Manager/Director(s) on the various tasks associated with conducting clinical trials.
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Master machine learning algorithms including forecasting, clustering, classification, reinforcement learning, recommendation systems, deep learning, etc. Master or PhD Degree (Preferred) in Electrical Engineering, Computer Science, Math, Statistics, Data Science, etc.
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For Associate Director: Minimum of 7 years of experience in Data Management in pharmaceutical clinical trials (preferably 3+ years from a pharmaceutical company and the rest from CRO, or research centers.
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Extensive experience with AWS or Microsoft Azure, and either Snowflake or Databricks is mandatory. Collaborate with senior leadership to integrate data strategy into the overall business strategy. Minimum of 10 years of experience in data management, data strategy, or a related field.
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Experience with Supply Chain Systems (SAP, MES (PAS-X), eLIMs, OMP, OSI-PI Historian). Learn more at Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy.
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Skills required Strong business andor technical background in the areas of Master Data Management Data Quality Data Governance Data Integration ETL SoA and Data Security. Deliver endtoend master data management projects for our customers that includes but not limited to Designing data model MDM Hub configuration.
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The primary responsibility of the MSL is to facilitate mutual exchange with Investigators, Thought Leaders (TLs), and Healthcare Providers (HCPs) to align interests, discuss research and medical information, and to facilitate clinical trial efforts.
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The research portfolio of the Dermatology Service includes optical engineering, artificial intelligence, basic science, translational science, epidemiology and clinical trials with over $5 million of annual funding from NIH, Foundations, Industry, and philanthropic sources.
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This position is responsible for designing and maintaining the existing file transfer system MFT product and modules such as Axway, Informatica Enterprise MFT, GoAnywhere, AWS Transfer Service,Knowledge of File Transfer design patterns and data engineering best practicesExperience with AWS data-related services such as EMR, Glue, S3, Lambda.
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OneOncology’s non-exclusive clinical trial site management subsidiary, OneR, delivers complex, multi-center clinical trials to affiliated practices. The practice offers Hematology/Medical Oncology, Breast Surgery, Palliative Care, Radiation Oncology, and Clinical Trials & Research Programs.
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Develop and file, in tandem with the General Counsel and the Compliance Office, mandatory insurance regulatory filings related to ERM, including but not limited to the Enterprise Risk Report and the Own Risk and Solvency Assessment (ORSA) Summary Report.
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trials trial master file jobs Title: trial master file in Warren, NJ
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