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Knoledge in Databricks, PowerBI, programing languages including SQL, Python and PySpark, data principles including data pipeline, streaming data, data storage, ETL, data integration, database design Leadership (Vision, strategy and business alignment, people management, communication, influencing others, managing change.
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Provides ad-hoc programming support to Clinical Operations, Data Management, Statistical Programming, Biostatistics, Drug Safety, Clinical Science, Medical Writing and Drug Safety to ensure rapid access to clinical study data for data cleaning/validation, SAS listings review, TLF, dry runs, etc.
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Proficiency in statistical programming languages (e.g., SAS, R) and clinical data management systems (e.g., Medidata Rave, Oracle Clinical) is essential. The Senior Vice President (SVP), Head of Data Analytics leads a multidisciplinary team responsible for biostatistics, statistical programming, and data management.
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Professional Certification (Security+, Data+, Cyber Security Analyst+, or Systems Security Certified Practitioner) Cyber Data Science (CDS) is looking for a data-focused professional with cyber security experience to join our new and growing team.
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Serve as a leader within the QC group and as a knowledge resource (data review, electronic review, data integrity, GDP) within the company. QC Testing data review of products, raw materials, stability lots.
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Critical aspect of the role includes defining an agile quality and compliance strategy that supports Digital Data unit in their effort to establish a standardized, resilient, and sustainable data pipeline - including data sources, data quality, data governance, data management and master data management.
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Employ CBA data visualization and editing tools to aid in the efficiency of gap analysis in CBA development, generating Joint Capabilities Integration and Development Systems (JCIDS) products, and provide a persistent data model that will reduce the need to re-create data across multiple program documents, and will feed requirements documentation, allocation, and tracking tools such as Dynamic Object-Oriented Requirements System (DOORS.
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By applying, you consent to your information being transmitted by Jobcase to the Employer, as data controller, through the Employers data processor SonicJobs. Strong background in electrochemistry, rechargeable battery chemistry including Li-ion, Na-ion, and solid-sate batteries, and energy storage systems.
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At J.Jill, our success is guided by a culture that values the intrinsic art of creativity and the data science required to drive our future growth. We are collaborative and data-centric, with every associate focused on creating our customers unique experience and delivering results through our omnichannel business model.
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The Director, PK/PD/PMX will provide scientific leadership through analysis and interpretation of PK/PD and dosimetry data in support of preclinical, translational, and clinical studies and programs.
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Demonstrated proficiency with data science languages (R, Python, SQL, Julia, SAS) and visualization tools (Tableau, Spotfire, SAS, JMP, RShiny) The Clinical Data Analyst partners cross functionally to identify risk to data integrity throughout the data flow to drive quality collection for non-EDC data sources (fluid & tissue labs, digital, imaging, wearables) in Dyne's clinical studies.
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Utilize knowledge of clinical data research methods, such as Trial Master File (“TMF”) to track critical clinical research documents and ensure proper recordkeeping and filing according to federal and global regulatory standards.
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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) Direct experience with different Data Management systems and technologies, Electronic Data Capture systems and CDISC data standards.
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Perform assay data review. Compile data and prepare graphs for documentation of test procedures and preparation of reports. BS or MS in a related science such as a Biology or Biochemistry is required SDS-PAGE, HPLC,CE- SDS, ELISA, Cell Based Bioassay, etc.
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Deep understanding of drug development, study conduct processes, GCP and regulations related clinical data management as well as ICH guidelines, FDA/EU regulations. Organize and direct the initial stage of the studies, review and sign off on various items such as eCRF, data validation, data review guidelines, and data management plans.
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data job Title: assistant Company: Focusgroupjobs in Lexington, MA
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