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Work closely with scientists within the in-vivo pharmacology group to verify in-vivo and Pharmacodynamic (qPCR) data. Work closely with scientists within the ADME group to verify bioanalytical data generated using HPLC-FD and LC-MS/MS.
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Familiarity with regulatory guidelines and standards related to bioanalytical data review. Job Title: Data Quality Control Specialist/ Operational Data Steward. Interpret data and provide insight for in-vivo studies, ensuring alignment with study objectives and protocols.
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Bioanalytical Data reviewer/ Quality Control - Contractor. Operational Data Steward – Lexington, MA. Enhance QC initiatives through the identification and implementation of best practices in data review and analysis.
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Familiarity with Bioanalytical sample and data analysis. Minimum of 1 year experience with data review/QC, preferred 3-5 years of experience. Experience being responsible for quality control of all scientific data generated within the Nonclinical Pharmacology group.
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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.
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The Senior Vice President (SVP), Head of Data Analytics leads a multidisciplinary team responsible for biostatistics, statistical programming, and data management. Proficiency in statistical programming languages (e.g., SAS, R) and clinical data management systems (e.g., Medidata Rave, Oracle Clinical) is essential.
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As part of the Clinical Operations organization, and within the Clinical Data Management team, the Senior Manager, Clinical Data Management is a critical role to ensuring the highest quality clinical trial data is available to support company objectives and claims.
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Demonstrated proficiency in drug safety databases (e.g., Argus), electronic data capture systems, and coding with MedDRA and WHO Drug dictionary. Job Overview: This role will be responsible for managing drug safety data, authoring safety documents, organizing meetings, collaborating with cross-functional teams, ensuring compliance with global drug safety regulations, and providing vendor oversight.
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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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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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The Human-centered AI team in Digital Health Oncology R&D is looking for an Associate Director of Data Science to specialize in the development of novel digital endpoints using data science, statistical learning, and innovative machine learning methods on multi-modal datasets including clinical data, real world evidence, imaging, wearables, and other biomedical data sources to address patient burden.
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The Field Application Scientist will be expected to develop relationships with key customers and KOLs and generate data and application notes that can be used in the sales process. We are focused on bringing to market a novel ultrasensitive immunoassay platform capable of utilizing small sample volumes with excellent data quality.
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Essential Experience & Job Requirements 5+ years of IT experience with major focus on data warehouse/database related projects Must have exposure to technologies such as dbt, Apache Airflow, Snowflake.
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Proficiency in data analysis and experimental design utilizing Minitab and Excel VBA code preferred. This will require fundamental knowledge of different synthesis methods and equipment, a deep knowledge of electrochemical techniques, and hands on experience with varying analytical techniques with a sound technical understanding of how to interpret the data.
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Leverage In-depth knowledge of Data Recovery, Business Continuity Plans, critical infrastructure management, incident response, vulnerability management, and data protection to ensure Voyager's security.
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data job Title: senior manager Company: Takeda Pharmaceutical in Bedford, MA
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