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Provide PV staffing for each Product Development Team and coach/supervise the staff in the execution of their responsibilities to the team as they pertain to drug safety including protocol input, Investigator Brochure input, annual reports, signal detection and the key safety components of potential NDA/PMA submissions.
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Amgen is currently seeking a Process Development Sr Principal Scientist in our Pivotal Attribute Sciences Department in Cambridge, MA. This team plays a crucial role in pivotal phase analytical development, including method development, validation, transfer, process and product development support, and GMP testing of drug substances and drug products.
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As a BA scientist, you will provide drug discovery and development bioanalytical input and support for the analysis of in vivo PK, PD, and in vivo samples across the global Oncology portfolio.
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Exceptional matrix team leader, ability to interface with leaders across the enterprise and project teams to develop long range plans and budgets for clinical biomarker pathology technologies aligned with company objectives, identify, pilot and establish new pathology related technologies to meet drug development needs in Ph 1, Proof of Mechanism/Concept, and in registrational clinical trials.
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PhD in Pharmaceutics, Biotechnology, Biomedical Engineering, Chemical Engineering, Biology or related field with a strong background in gene therapy-based drug product development and 3+ years industry experience.
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Some job boards have started using jobseeker-reported data to estimate salary ranges for roles. 3+ years experiences in model development or validation or financial analysis. Perform / lead independent review and model validation of wholesale credit risk and compliance risk models including PD, LGD, Loss forecasting, AML, Fair Lending, Fraud Detection, and other business or operational related models.
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The Senior Lead Data will be responsible for partnering with Technology, Machine Learning, Product Architecture, and other Capital One teams to support the development of the Finance Tech Data Strategy into products and services we create and consume.
$9 - $11Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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We are looking for a experienced quantitative credit risk professional that will participate and lead in design, development, testing and execution of credit risk models that cover CCAR/ DFAST Stress Testing, CECL (ACL), Economic Capital, BAU Loss Forecasting and other applications like lifetime loss for pricing for Bank’s Lending Portfolios.
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This position requires a solid understanding of clinical drug development, GCP and regulatory requirements for clinical trials process. Participate in the development of tools and the reporting of metrics for monitoring clinical study progress and surveillance of key efficacy and safety data points.
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The successful candidate will thrive in a proactive can-do culture and enjoy working across the full range of clinical development activities for the ground-breaking, mRNbased immuno-oncology-based new drug candidates in addition to being a highly-effective internal and external team player and terrific communicator and collaborator.
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Hands-on development experience with Design and Architecture of big data frameworks/tools: Azure Data Lake, Snowflake, Azure Data Bricks. 8+ years of related professional experience including 5+ years in data lake development in large reporting environment(s.
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Extensive ADME experience from target assessment to drug development. This team is searching for a Principal Scientist, ADME. You will be collaborating with the Preclinical and Analytical Sciences group, to manage ADME lab operations and support small molecule drug discovery programs for cardiovascular indications.
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This role will be responsible for driving the development and implementation of an enterprise data strategy and architecture, including implementation of systems, tools and processes to enable critical use cases in data lineage and lifecycle management, analytics and reporting, systems integration, and process automation.
$165,900 - $223,800 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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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. Develop data management SOPs and processes that align and address business priorities; Contribute to cross-functional SOP development.
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We are seeking a highly motivated and capable Data Scientist to support Tempus NEXT, an AI-enabled care pathway intelligence platform that applies technology, data, and AI to enable precision medicine, empowering providers to tailor the next step in a patient’s care journey and foster value based care within health systems.
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data drug development jobs Title: vice president in Cambridge, MA
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