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Demonstrated experience with a variety of relational database and data warehousing technology such as AWS Redshift, RDS, BigQuery, Databricks. Demonstrated experience with big data processing systems and distributed computing technology such as Databricks, Spark, Sagemaker, Kafka, Tidal/Airflow, etc.
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Working under the direction of the Administrative Manager, the Senior Surgical Pathology Coordinator will work at an advanced level and under general supervision to perform technical and clerical functions required for core front-end laboratory operations, clinical and administrative support to a director, faculty, and/or chief of service, database and materials management for clinical and research projects, calendar management, travel arrangements, and coordinates conferences and courses.
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We’re helping patients get the best care possible by working on digital health experience, analyzing big data to streamline the delivery of care, and reaching out to medically complex patients to better understand their needs.
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Experience in stream / data processing technologies like Kafka, Spark, Google BigQuery, Google Dataflow, HBaseFamiliarity designing CI/CD pipelines with Jenkins, Github Actions, or similar toolsExperience with SQL, particularly performance optimizationExperience with Graph and Vector database or processing frameworksStrong knowledge of data modeling, data warehousing, and data integration best practices.
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Works with the Executive Team, as well as the Development Assistant, to monitor the MAPS Client Database and address technical glitches, incorrect data entry, etc., that hinder users’ ability to retrieve data needed to support fundraising, grant writing and other efforts.
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Maintain data security and integrity, thorough monitored backups, database management, security management, and application auditing. This includes developing, maintaining, supporting, and optimizing key functional areas, network infrastructure, server infrastructure, data communications, and telecommunications systems.
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Manipulate raw product, inventory, or customer data (database, XML, XLS, CSV, JSON, etc.) into formats suitable for loading into various data stores – such as NoSQL databases, relational databases, or API-first third-party systems.
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Experience with BI software tools like Tableau, Qlik, PowerBI. Preferred Skills: IT skills, data governance skills, and analytics. Experience in Database capabilities such as SQL, PL/SQL for relational databases and NoSQL oriented databases like MongoDB, Cassandra.
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Responsibilities: The SAS Programmer is responsible for developing and executing biostatistical (SAS) and data management related programs, processing data from various sources to support clinical and pharmaceutical projects and will include defining populations, creating variables, developing various statistical models, program debugging, as well as supporting model implementation.
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Acts as front line for clinical research approval process within Division: Assists in coordinating clinical research review process, serves as initial contact point for Clinical Research Lab (CRL) related requests, maintains database of small-funding opportunities and maintains research resources on website and other internal online platforms.
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Net applications to be compatible with new database interface, including proxy classes, data bindings, connection classes, and connection strings. Core Qualifications: The candidate should have extensive experience using ADO.NET. Experience working with ADO.NET database connections, data readers, data tables and datasets.
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Maintain data integrity in compliance with GCP, relevant SOPs and regulatory requirements by reviewing data processes and filing documentation in the trial master file (TMF) Comprehensive understanding of database and dictionary structures (e.g., MedDRA, WHO DRUG.
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Experience working with a Pharmacovigilance database, with preference given to experience with Argus Global safety database. Collaborate externally with Drug Safety vendors and business partners on case management issues, processes, and timelines to meet global regulatory requirements for adverse event reporting and data exchange obligations.
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Oversee CRO and vendors, and participate in study start-up activities, including development, review, and approval of eCRF requirements, EDC database specifications, Data Transfer Specifications, eCRF completion guidelines, Data Management Plans, Data Validation specifications and User Acceptance Testing.
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Toolkits, SEIMs, Logrhythm, ACAS/Nessus/SCAP, mandatory/role-based access control concepts (e.g. SE Linux extensions to RHEL, PitBull, AppArmor, and Sentris), video teleconferencing/VOIP, Oracle/MS SQL database security, and Apache/IIS Web server security.
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data database jobs in Weston, MA
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