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Data Analytics and/or HEOR activities, with demonstrated strong methodological skills (study design, data analysis, and interpretation) in health services research. Expertise in Clinical Informatics or Health Information Technology (HIT), including working with claims data sets or Electronic Health Record (EHR) systems.
$205,400 - $342,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience could include any of the following: Direct patient care & outcomes, previous MSL or field medical plus Clinical, formulary, and/or other management experience, Managed Care, pharmaceutical industry, and/or Quality Improvement Data Analytics and/or HEOR activities, with demonstrated strong methodological skills (study design, data analysis, and interpretation) in health services research.
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The VP Global Head of Statistics for Vaccine Clinical Research and Development (VCRD) sets the vision and leadership for providing the highest level of data management, modelling, and statistical advice across the function to senior Vaccines Research and Development (VRD) leadership.
$239,300 - $398,900 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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You will manage the sourcing requirements for all phases of the sourcing process, including project identification and start up, data collection and analysis, option development and recommendation preparation, implementation and supplier management for site-based activities.
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In collaboration with Global Medical Affairs colleagues, partner with Worldwide Research & Development and Medical (WRD) and Global Product Development (GPD) in the identification of potential sites for Pfizer-sponsored clinical trials, including identification of sites serving under-represented patient populations in trials.
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You will collaborate with the Primary Pharmacology Group (PPG), hit follow-up, lead optimization, External Research Solutions, Medicinal chemistry stakeholders, and Digital and data support to ensure timely, high-quality access to the Pfizer compound collection while providing expert follow up support especially when troubleshooting potential workflow related issues in your pursuit to identify root cause to make quality improvement corrections.
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Outside of the Platform, the VP will work with leaders from Biostatistics & Data Management, Global Regulatory Affairs, Clinical Pharmacology / Pharmacometrics, HEOR, Legal/Compliance, and others to achieve research and business objectives.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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6+ (with a doctoral or similar degree) to 8+ (master degree), or 10+ (bachelor degree) years' experience with a proven successful track record of program or scientific management for partnerships / alliances, collaborations, innovation initiatives or major strategic initiatives for pharmaceutical, biotech companies, academic, or any other organization engaged in health, clinical or life science research enablement or quality improvement.
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BS + 20+ Years relevant experience Global Regulatory affairs, Pharma QMS Development and Management, Clinical Quality, GCP Auditing, Regulatory Inspections experience; MS, MSJ, MBA +18 years relevant experience; PharmD/PHD + 15+ years relevant experience; MD + 9+ years relevant experience.
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Clinical Development expert focused on team leadership in early planning and set up, the oversight of clinical studies execution in partnership with Pfizer preferred Clinical Research Organization (CRO)/Vendor responsible for the operational management of Pfizer Ignite clinical studies and team leadership of appropriate study reporting.
$161,600 - $269,400 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Appropriately provide medical support throughout the Investigator Sponsored Research (ISR) process Cultivate research and therapeutic area expertise, including familiarity with latest congress data and disease state literature.
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In depth understanding of the business of pharmaceutical medicine including clinical trial design, GCP and data interpretation, drug development, regulatory and promotional rules/guidance, legal and compliance, issue management and business development opportunity evaluations.
$117,300 - $195,500 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Provide education on the clinical and economic impact to help inform customer decision-making and improve population health through the communication of real-world data analyses, pharmacoeconomic analyses, outcomes evaluations, and medical presentations.
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