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This is a unique opportunity for an experienced biostatistician leader to join Scientific Insights & Analytics group (Biometrics & Scientific Communications) in the Surgical Structural Heart Valve (SURG) business unit to support various global medical and clinical activities.
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Acting as core team member/lead biostatistician for clinical trials with the team and cross functionally. PhD in Statistics or Biostatistics or related field with 8 years of previous analytical experience in clinical trials or clinical research.
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Accountable for planning, design, execution, and results of the Clinical Affairs Biomarker team & clinical trials program. Interact with R&D, Marketing, Regulatory, Medical and Scientific Affairs, and other global functions as well as senior leadership teams and global partners to apply advanced critical thinking to build strategic plans for new biomarker development, stakeholder management, and technology dissemination such as Real-World Evidence, ensuring benefit from the new capabilities and opportunities these enable.
$185,500 - $235,500 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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The Clinical Affairs Director for Beckman Coulter Diagnostics is responsible for leading comprehensive global clinical trial strategies to support the complex Clinical Chemistry and Immunoassay Biomarker-Flywheel (Biomarker) program and for managing a multi-level team of clinical managers and clinical scientists/affairs associates.
$185,500 - $235,500 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Clinical chemistry, immunoassay FDA & EU or Class III medical device experience with broad knowledge of medical device industry, regulatory requirements, and frameworks. This position is part of the Chemical Chemistry and Immunoassay (CCIA) Clinical Affairs department located in Chaska, Minnesota and can be remote.
$185,500 - $235,500 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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5+ years of work experience in technology enablement for clinical trials, scientific leader engagement and/or real world evidence generation. Be the chief advocate and evangelist within the widerorganization for Clinical & Real-World Evidence Generation products to drive adoption, fantastic user experience, and value realization.
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The Executive Director, Clinical & Real-World Evidence Generation Product, is responsible to deeply understand the needs of our partner organization, develop and evolve a vision for the suite of products and associated services of the value team, and lead a cross functional team to the successful realization of that vision.
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Ensure all appropriate CMC regulatory aspects for clinical trials/product release are in place, to avoid clinical holds and/or to ensure continuity of market supply. Drive the CMC Regulatory strategy to support development, registration, and early post approval activity, in accordance with the applicable regulatory & scientific standards, and taking into account the evolving regulatory requirements.
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The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director.
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Assist the Deputy Director in accelerating the transfer of technology from academic or industry project teams in preparation for new clinical trials. This position will primarily be responsible for the strategic design, validation, and implementation of new Quality Control technologies to optimize efficiency, increase adherence to quality standards, and/or prepare for new clinical trials.
$61,046 - $95,972 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Clinical & Real-World Evidence Generation (CRWEG) Value Team brings together product, engineering, and data expertise to drive the data and technology strategy that accelerates our company’s ability to develop innovative medicines that change the course of human health.
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Cardiovascular & Metabolism Regional Medical Scientific Director's liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies.
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Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities.
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Fresh PhD with 3+ years’ experience or MS with 5+ years’ experience in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience.
$121,000 - $152,000 a yearPart-timeExpandUpdated Today - UpvoteDownvoteShare Job
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Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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