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Oversee quality assurance activities to ensure the integrity, accuracy, and compliance of clinical trial data within Veeva Vault applications, in accordance with regulatory requirements (e.g., FDA guidelines, GCP standards.
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Current certifications in any of the following areas: cloud provider (AWS, Azure, GCP) technologies, cloud data technologies (Redshift, BigQuery, Synapse, Fabric, Snowflake, Databricks, etc.) Minimum 2 years of practical experience with at least one of the three major cloud providers (AWS, Azure or GCP.
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Familiarity with cloud platforms like AWS, Google Cloud Platform (GCP), or Microsoft Azure. Headquartered in San Diego and with employees across the globe, Seismic is the global leader in sales enablement , backed by firms such as Permira, Ameriprise Financial, EDBI, Lightspeed Venture Partners, and T. Rowe Price.
$237,100 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The modern data stack building includes consolidation across multiple applications (like Salesforce, SAP, Oracle, IBM, AWS, Azure, GCP, Databricks, Qlik, Power BI) at scale (Terabyte to Petabyte volume, 10M+ customers/users.
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You will use tools such as GCP BigQuery, Looker Studio and Power BI to extract data and create reports for ad-hoc and routine reporting. Software Experience: Knowledge of SQL, SAS, R, Python, Tableau, GCP, and/or other programming/data query/reporting knowledge, also, intermediate to advanced skills in Microsoft Excel is required.
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Design and oversee the implementation of quality systems specifically for CMC development activities, including the release of products for GLP and GCP studies. Establish robust processes for the review and release of products intended for GLP and GCP studies, ensuring data integrity and compliance.
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Job DescriptionDirector, R&D Quality, GCP - Cell Gene Therapy (CGT)The Director of R&D Quality, GCP - Cell Gene Therapy (CGT) reports directly to the Head of RDQA and is a trusted advisor and partner to clinical and quality stakeholders and business partners and supports the program and study level quality leads in key quality related clinical activities and deliverables for all CGT programs across the Vertex clinical portfolio.
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Scripting/coding experience of continuous delivery (CD) GitOps practice with tools such as ArgoCD, Jenkins, CircleCI, or Spinnaker in deploying and maintaining services in AWS, Azure, or GCP cloud.
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Familiarity with AWS, GCP, Databricks, Github, Airflow and Looker. Familiarity with AWS, GCP, Databricks, Github, Airflow and Looker. Identify and analyze new fraud detection features using SQL, Databricks, and Python.
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As a Lead Cloud Architect, you will be responsible for overseeing the migration of various applications and portfolio applications from their current environments to AWS, Azure, OCI, and GCP cloud platforms hosted in FedRAMP and FedRAMP+ environments.
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Role OverviewThe Human Research Compliance Specialist (compliance auditor) provides education and support to researchers and is responsible for performing audits of IRB-approved clinical research protocols across our institutions to ensure compliance with FDA, OHRP and other state and government regulations, Good Clinical Practice (GCP) guidelines, as well as with our organization's clinical research policies.
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Lead identification of assay requirements, lab selection, and contract development to ensure regulatory compliance according to GLP, GCP, and applicable global regulatory requirements such as CLIA and EU IVDR, and execution feasibility.
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Locations: VA - McLean, United States of America, McLean, VirginiaSenior Platform Engineer (GCP/AWS) 3+ years of experience in Identity Platforms such as Ping, Okta, or Radiant Logic. Manage enterprise identity cloud directories including Microsoft Azure AD, AWS Microsoft AD, and Google Cloud Domain Directory.
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Authoring and maintaining IaC with Terraform and using IaC to deploy resources in AWS, Azure, GCP, or any other public cloud providers; Data warehousing tooling and services (Apache Airflow, AWS DMS, Snowflake.
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Knowledge of GLP/GCLP and GCP global regulatory requirements for clinical trial submissions (USA, UK & EU), understanding of 21CFR Pt. 11 with respect to clinical systems (QMS). Extensive experience managing deviations, RCA and CAPAs in a GLP/GCP environment.
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gcp job Company: Ppd in Boston, MA
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