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Outside of the RWE organization, the VP will work with leaders from other CMAO functions, Biostatistics & Data Management, Global Regulatory Affairs, Clinical Pharmacology / Pharmacometrics, HV&E , Legal/Compliance, Worldwide Medical and Safety, and others to achieve research and business objectives.
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Supports multiple aspects of resource and clinical development cost management including data transformation, analysis, and reporting. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
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Experience using project and/or resource management systems and reporting tools (e.g., Microsoft Excel, Microsoft Project, Business Objects, Spotfire, Planisware (preferred), etc) Demonstrated understanding of the both the Early and Late stage drug development process portfolio management and resource planning.
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Executes clinical research studies in accordance with scientific, medical, and ethical principles, within regulatory requirements/guidelines, and Pfizer SOPs. The Clinical Research Nursing Provider is a member of the Pfizer Clinical Research Unit which is a global organization with Clinical Research Units in New Haven, CT and Brussels, Belgium.
$31.82 - $53.04 an hourFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Reports to the Sr. Director, Scientific Planning and Operations to partner with the Pfizer Ignite Operational Leads and Pfizer Ignite Clinical Study Team Leads (iCSTLs) in the Ignite SSO group to perform project management and coordination, meeting planning, and business planning activities.
$74,900 - $124,800 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Clinical, formulary, and/or other management experience. Appropriately prioritize the needs of the customer and of Pfizer to develop and implement objective and scientifically sound Real World Evidence-based outcomes tools (such as HOPEs and educational programs) which identify the greatest opportunities for improving patient care, closing quality gaps, and addressing population health management.
$205,400 - $342,400 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Has extensive understanding of related disciplines, e.g., clinical operations, safety, biostatistics, regulatory, study management, pre-clinical, pharmacology, quality assurance. Science degree (PhD, PharmD) and minimum of 9 years Clinical Research experience in industry/CRO.
$161,600 - $269,400 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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You will partner with key stakeholders and colleagues in Clinical Pharmacology, Quantitative Systems Pharmacology, Statistics, Translational Modeling and Simulation, and other Research and Development lines to accelerate breakthrough cancer medicines that bring new hope to patients everywhere.
ExpandApply NowActive JobUpdated 22 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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Resource Operations Associate provides operational resource support to the Resource Strategy & Operations Organization in the support of the Research, Development and Commercial portfolios are properly planned and understood to facilitate informed decision-making and allocation of resources based on business priorities.
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