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The OHDA team collaborates with the Epidemiology department, the Janssen Research and Development organization, and others within the Johnson & Johnson Family of Companies on generating and disseminating real-world evidence about disease, health service utilization, and the effects of medical products through the analysis of healthcare data.
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Develop and lead North American evidence generation strategies and execution, including Real World Evidence, Health Economics and Outcomes Research, Investigator Initiated Studies, Collaborative Research and Corporate Sponsored non-registrational studies.
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Drive impactful publications, evidence dissemination and scientific/medical communications. Contribute to the development and execution of Global Medical Affairs Medical Strategy Documents and Evidence Generation plans.
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Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
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In this exciting role you are an individual contributor joining our Real World Evidence team in Medical Affairs, with a dotted line into our Biostatistics and Clinical Data Management Department working within GRAIL’s Clinical Development organization.
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This position provides high quality statistical programming analysis and reporting and regulatory submission deliverables for Real World Evidence projects across our company's Biostatistics and Research Decision Sciences (BARDS) group.
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This position will be responsible for supporting and contributing to the development and execution of robust health economics, outcomes research, epidemiology and real-world evidence plans that are aligned with brand strategies, medical affairs strategies, clinical development plans, support product value propositions, and optimize market access.
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This project will require research into the current regulatory guidelines, the landscape of specific therapeutic product(s) information in the public domain, interpretation, and acceptability of utilizing Real World Evidence (RWE) to fulfill the requirements.
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We are currently seeking a Real World Evidence (RWE) Director to join our HEOR team. Our data analytics and software platforms support data science, commercial operations, real world evidence, and cloud information management.
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We are currently seeking a Real World Evidence Method Research Intern. This internship offers an excellent opportunity to gain practical experience in the rapidly growing field of Real-World Evidence.
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Further, they will be a strategic thought partner to the CTS leadership team in developing the overall Real World Evidence strategy and products. The Associate Vice President of Real World Evidence is responsible for contract achievement and revenue delivery of CVS Real World Evidence business.
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Provides global medical leadership to drive alignment to the GIET medical strategy across all phases of product development, and include all activities (insights, unmet needs, preclinical and clinical research, investigator-initiated studies, registries, real world evidence, market access, professional education), to ensure launch excellence.
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The MEL conducts critical activities that support advancing science, educating on evolving clinical practices, transforming science into patient care, and facilitating the development of new research collaborations (including Investigator Initiated Trials and Real-World Evidence.
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Foster and identification of key opportunities for scientific growth and medical evidence generation for the support of current approved products with a focus on Real World Evidence.
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Changes in healthcare systems with advances in medicine and health technologies have accelerated the use of Health Economics and Outcomes Research (HEOR) and Real World Evidence (RWE) to support decision making on adoption of our innovative therapies across multiple stakeholders.
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