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Experience with statistical analysis including statistical, data analysis, and data visualization tools such as SAS, SQL, R, Python, Tableau, Looker or similar. As part of our Digital & eCommerce (D&eC) organization, you will have the opportunity to work on the leading website in the life science industry to shape the overall customer experience and support the development of our digital strategy based on data-driven insights.
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Prior designation as a Data Protection Officer (DPO) supporting European privacy operations required. Partner cross-functionally with business stakeholders and IT to support the administration of system risk assessments and associated data protection impact assessments.
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The Associate Medical Director/Associate Scientific Director provides specialist medical/scientific strategic and operational input into core medical affairs activities within their TA, inclusive of healthcare professional/provider interactions; generation of clinical and scientific data; educational initiatives (medical education, data, guidelines and value proposition); safeguarding patient safety (risk minimization activities / safety surveillance activities.
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This role represents the CP Expert Team to the global cross functional drug discovery and development project teams, in close collaboration with colleagues in Biostatistics, Data Sciences, Clinical Biomarkers and Diagnostics, Research, Clinical Development and other colleagues within the R&D organization.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Act as the medical monitor for clinical studies, reviewing patient data on an ongoing basis and meeting with investigators to develop an understanding of the safety profile and antitumor activity of new immuno-oncology agents in development.
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Strong technical background, with demonstrated ability to partner effectively with engineering, designers, UX, and data science. Leverage data to understand risks, impacts, scope and priorities of our business objectives, and enable the team to drive results.
$224,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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MentGeneral familiarity with biostatistics and/or pharmacometrics; expert in navigating scientific literature, interpretation of data, display of. iesResponsible for the strategic planning, authoring, and review of the translational biology components of regulatory documents, scientific data and publicati.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Reporting to the Senior Director, Clinical Data Management, the Associate Director, Clinical Data Management will define and lead the clinical data management strategy for the organization.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Reporting to the Head of Safety, the Senior Medical Director, Drug Safety will lead pharmacovigilance activities including the analysis of safety data, identifying, detecting and investigating safety signals, evaluating and proactively managing risk, and providing medical safety review of Dianthus products.
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For positions requiring access to technical data subject to export control regulations, including Export Administration Regulations (EAR), ServiceNow may have to obtain export licensing approval from the U.S. Government for certain individuals.
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He/she will be responsible for designing and initiating clinical trial(s), supporting clinical data review, interpretation of study results and drive a compound through development. Plan and lead ongoing medical data review in collaboration with data management and other functions.
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We provide investment servicing, data & analytics, investment research & trading and investment management to institutional clients. If you like change and innovation, seek to see the bigger picture, make data driven decisions and are a good team player, you could be a great fit.
$267,500 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Associate Director, Clinical Data Management is responsible for overseeing the start-up and execution of multiple, complex trials with a CRO and supporting upcoming submissions. 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.
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Drive state-of-the-art multi-parameter medicinal chemistry optimization with creativity, innovation, in-depth analysis of data, and existing literature information. Proven ability as chemistry leader on validating or prioritizing targets with conclusive data package.
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Oversee the collection, analysis and interpretation of clinical trial data, working closely with Clinical Development, Biostatistics and Data Management teams to ensure data accuracy and integrity.
ExpandApply NowActive JobUpdated 30 days ago
data job Title: director in Bedford, MA
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