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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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Previous experience in data analytics and tools (i.e. SQL, Tableau) is highly desired. The position requires knowledge of quality systems, statistical tools, lean six sigma methodologies, process capability, and understanding of control plans and process flow.
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Knowledge of data management practices across the full data life cycle, such as data strategy, requirements, design and development, data science, data governance, metadata management, data quality, business intelligence, and data security & privacy.
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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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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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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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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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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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This role will collaborate with the Clinical Operations and Clinical Development team, and with other functions as applicable, to ensure project deliverables are met, including data acquisition, quality data review, and reporting in compliance with GCP, SOPs, and regulatory requirements.
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Ensures prompt, quality responses to Institutional Review Boards (IRB)/Ethics Review Committees (ERC), Independent Data Monitoring Committees (IDMC), etc. Ensure delivery of quality study strategy and design, understand the analysis and interpretation of data throughout the study.
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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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Demonstrated success with domestic and international consulting, permitting, licensing, and environmental quality review processes for a wide range of infrastructure projects in sectors such as power generation, process industries, water/wastewater treatment, telecommunications, data centers, and industrial manufacturing.
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Strong background in using HR data and HRIS products desired and experience producing analytics containing sensitive information and high levels of accuracyExpert level in ExcelExperience with Business Intelligence tools, i.e. Tableau, Domo, etc.
$60,400 - $75,500ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Support the development and maintenance of quality systems and processes related to assay development and validation. Strong analytical and statistical skills, with experience in data analysis software (e.g., JMP, Minitab.
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Perform biologics quality assessment utilizing a variety of techniques, such as CE-SDS, SEC-HPLC, and endotoxin assay. Experience in various imaging/multicolor flow cytometry-based instruments and data analysis programs.
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data quality jobs in Concord, MA
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