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Experience being responsible for quality control of all scientific data generated within the Nonclinical Pharmacology group. This position is responsible for the quality control of all nonGLP data generated in the Nonclinical Pharmacology group within GNAT unit of client.
$32 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Bioanalytical Data reviewer/ Quality Control - Contractor. This position is responsible for the quality control of all nonGLP data generated in the Nonclinical Pharmacology group.
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Serve as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all CDS activities including selection and application of data acquisition standards, Data Management Plan, selection of quality risk indicators, third party study data due diligence.
$84,200 - $155,900 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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This position is responsible for the quality control of all nonGLP data generated in a Pharmacology group. The role is focused on Data Quality Assurance/Quality Control.
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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.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Summary: This position is responsible for the quality control of all non-GLP data generated in the Nonclinical Pharmacology group. Prior experience in quality control of Scientific data.
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Assist with performing non-destructive testing to ensure quality and detect defects; methods include: Visual Inspection, Ultrasound Testing, and Magnetic Particle Testing. Nova Data provides both on the job and classroom training and development to further our employees' careers as an NDT Technician.
$16 - $22 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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DPS Group is seeking a qualified Senior Quality Assurance Operations professional to perform batch disposition, batch record review, deviation, CAPA and change control support at the Boston, MA client site.
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Comprehensive Knowledge of Master Data Management (MDM), data governance, and data quality business processes, solutions, and methodologies. Experience with 3rd party pharmaceutical data like IQVIA (IMS Health) Sales Data (DDD, Xponent, NSP, NPA), Affiliation (HCOS), APLD (Medical Claims), and Specialty pharmacy data.
$169,400 - $266,200 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Data Steward leads complex, cross-organizational conversations – including risk assessment, data quality auditing, issue management, and knowledge management – to ensure Claims Transaction data is fit for organization use.
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Support data review of cell therapies, AAV products, and Critical Components. Experience in data review, organization, and analysis using statistical software. They will actively collaborate with research, process development, quality teams, regulatory and CDMOs to ensure a compliant stability program in addition to providing Quality Control support to ongoing CRISPR Tx programs.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Associates, Bachelors, or Masters graduate with 1+ years of experience in a quality control environment performing data review/analysis of chromatography and spectrometry methods. Ensure data integrity and quality by adhering to internal and other regulatory guidelines.
$25 - $32 an hourExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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The relevant infrastructure will include elements such as an enterprise data catalog, data governance (including conventions and standards), data quality, master data management, application integration, data exchange, ETL/ELT, data modeling, and related components.
$165,900 - $223,800 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Represent QA / QC on project teams, as needed and provide GMP compliance interpretation, consultation, and other supportive services necessary to maintain and improve compliance to ensure product quality, data integrity and patient safety.
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Minimum of 6 years of experience in drug safety/pharmacovigilance quality assurance or compliance within the pharmaceutical or biotech industry. Certification in pharmacovigilance (e.g., RQAP-GLP, PVQA) or quality management (e.g., ASQ Certified Quality Auditor) is a plus.
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data quality jobs in Woburn, MA
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