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The Associate Director/Director, a member of Shionogi's Global Epidemiology and Real-World Evidence (GEE) team, is responsible for strategizing and generating real-world evidence using fit-for-purpose data to support global products at each stage of the product lifecycle.
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In-depth knowledge of statistical methodologies, clinical trial design, and real-world evidence generation, with a focus on optimizing study design and data analysis. This key leadership position involves providing guidance and expertise in statistical methodologies, study design using real-world data to facilitate and support development and regulatory interactions of pharmaceutical products.
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MD, PhD, MPH, PharmD, RN or PA with at least 5 years’ experience in Epidemiology, Health Economics Outcomes Research (HEOR), or/and Health Systems Research. Project management oversight – ensuring effective design, initiation, and implementation of real-world evidence studies, while ensuring effective study protocols and plans, managing budget and milestone tracking, and, where appropriate, contracting with partner organizations.
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Particularly noteworthy opportunities for undergraduates include the Charles A. Dana Research Institute for Scientists Emeriti (RISE), the Drew Summer Science Institute (DSSI), the Center for Civic Engagement, as well as seven New York City semesters and several international study abroad programs.
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Strong familiarity with study start‐up activities, including feasibility, country and site activation, patient recruitment. Provides operational support for the Clinical Operations team with heavy focus on study start‐up activities, patient recruitment efforts, maintenance, and study closure deliverables.
$96,000 - $134,667 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Experience teaching within a higher education institution; preference given to those able to teach across the curriculum, though a focus on biostatistics, epidemiology and global health are strongly preferred.
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A Juris Doctorate (JD), Master of Laws (LLM), or Master's degree in Accounting or Taxation field of study will be considered in lieu of a Bachelor Degree in Accounting. A Juris Doctorate (JD), Master of Laws (LLM), or Master's degree in Accounting or Taxation field of study will be considered in lieu of a Bachelor Degree in Accounting.
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Study Strategy: Provides the strategic direction to Biostats Data Mgmt & Data Ops for EDC, edit checks, data quality listings, SAP, Data Mgmt plan; Reviews patient population and protocol compliance for consistency with study strategy; Develops biomarker strategy in collaboration with Translational Medicine/Clin Pharm; May act as Clinical study leader (CSL.
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The research portfolio of the Dermatology Service includes optical engineering, artificial intelligence, basic science, translational science, epidemiology and clinical trials with over $5 million of annual funding from NIH, Foundations, Industry, and philanthropic sources.
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We are currently hiring for Manager/Senior Manager level professionals for our Decision Science practice who have expertise in Patient/Epidemiology based forecasting within Biopharma/Oncology. Candidates will be expected to have expertise in managing & developing Patient/Epidemiology based forecasting models for pharma clients within Biopharma/Oncology.
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Understanding of clinical trial and real-world evidence study design and execution, statistical methods, and reporting requirements. This may include but is not limited to documents prepared by FDA, OIG, DDMAC/OPDP, PhRMA, ICMJE, ACCME, etc.
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This course is a study of the earth's structure, composition and history; processes which shape the earth's surface, such as glaciation, crustal movements and tectonics, erosion, and sedimentation; fossil study; classification and characterization of rocks; applied geology of mineral, energy, water and ocean resources; and of natural hazards.
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Useful additional degrees: Post-graduate degree in Pharmaceutical Medicine; Master of Public Health in Epidemiology (or equivalent) strongly preferred. At least 10 years in drug development in a biotech or pharmaceutical company, including a minimum of 8 years in a safety-related position.
$240,000 - $333,333 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Assist with study start up and maintenance activities relevant to regulatory affairs, as needed. Assist with study start up and maintenance activities relevant to regulatory affairs, as needed.
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Leads the task of establishing study-specific work procedure for reporting Anti-Drug Antibody data from bioanalytical lab to clinical sites. Manages memberships, facilitates meetings to assemble study deliverables at multiple decision points in the Global Drug Development Process and authors meeting summary across multiple PrM sub teams.
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epidemiology study jobs in Basking Ridge, NJ
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