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Develop and execute Medical Affairs sponsored clinical programs, including but not limited to Phase 3b/4 trials, registries, real-world evidence studies, investigator-initiated and/or collaborative studies in the Dermatology TA. Contribute/ lead study design, protocol development, clinical study report and publication development.
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The Director, Epidemiology would be responsible for oversight of various projects and initiatives in areas of epidemiology and real-world evidence research. Identify research study needs, drafting proposals and protocols, and contribute to real-world evidence (RWE) strategy and study conduct across the Oncology portfolio.
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Ensure quality of design, execution, and publication of real-world evidence studies, and quality of models & tools developed for business partners. Collaborate with internal and external experts to generate rigorous scientific data, and contribute to the development of dissemination plans, as aligned with the Integrated Evidence Team (IET), to support the RWV&E strategic plans for the assigned therapeutic areas.
$65.99 - $72.99 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The GPD will be responsible for the leadership of direct reports and must work closely with multiple functions including TALVEY Marketing/Market Access Team, Strategic Customer Group (SCG), Franchise Marketing and KAMs, Sales, Sales Training, Business Analytics, Medical Affairs, Real World Value & Evidence (HECOR), R&D, Corporate Communications and outside vendors to effectively execute key commercial activities.
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The mission of the Safety Surveillance & Collaboration (SS&C) team, CVS Health Real World Evidence, is to actively monitor the US public health in collaboration with Food and Drug Administration (FDA), academic institutions, and other health insurance companies.
$124,372.5 - $247,200 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Represent RWV&E on cross-functional teams with business partners, such as Real World Analytics and Alliances, Marketing, Medical Affairs, Strategic Customer Group, Global Commercial Strategy Organization, Commercial Excellence, Epidemiology, Government Affairs and Policy, New Business Development and other Operating Companies, as needed.
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In this position, the Contractor, RWV&E, will be responsible for conducting RWV&E evidence generation and dissemination activities for assigned therapeutic areas, pipeline and marketed products or indications, within the Company Oncology Franchise.
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Designs, implements, and disseminates a portfolio of prioritized real-world evidence/outcomes research studies and outcomes research activities linked to value and implementation goals. Designs, implements, and disseminates a portfolio of prioritized real-world evidence/outcomes research studies and outcomes research activities linked to value and implementation goals.
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Collaborate with internal and external experts to generate rigorous scientific data, and contribute to development of dissemination plans, as aligned with the Integrated Evidence Team (IET), to support the RWV&E strategic plans for the assigned therapeutic areas.
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Interact with Regional Market Access/Health Economics / Outcomes Research and Medical Affairs teams to coordinate and develop real world evidence generation in support of their access programs.
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Target Buyers: Clinical Operations, Regulatory Affairs, Medical Affairs, Real World Evidence, Real World Data Owners, Medical Operations, Outcomes Research, Health Economics. At UBC, we provide services to enhance the entire drug development process and commercialization lifecycle - from clinical trial support to real-world evidence generation.
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A master’s degree in health economics, statistics, health policy, pharmacy or related field is required. Experience in the pharma or healthcare industry is preferred, in health economics, market access or related research functions.
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