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As a core member of the Medical Sub-Team (MST) on the Global Product Team (GPT), the incumbent will be accountable for establishing the Scientific Communication Platform (SCP) for products in their Therapeutic Area, and ensuring alignment of each product’s overall scientific content/communications strategy reflect the input and requirements of relevant Pfizer Oncology stakeholders (e.g., Medical Strategy, Field Medical, Clinical Development, Scientific Affairs, Research, etc.
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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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Work with Pfizer Oncology Scientific Affairs to develop communications for non-medical audiences e.g., Board, Investor Relations, etc. Support GPTs, Global Medical franchises, and other Pfizer Oncology stakeholders in engaging with the external medical community on publication activities related to key clinical trial data readouts.
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The ECS Clinician will work with other functional disciplines as needed (e.g. Research Unit clinicians/Global Clinical Leads/Medical Monitors, Biostatistics, Clinical Pharmacology, Precision Medicine, and Digital Medicine.
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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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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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Support development of HIT/clinical informatics specific resources for field medical colleague use. 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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Develop expertise working with Pfizer clinical checklists and Standard Operating Procedures (SOPs) to ensure compliance with good clinical practice (GCP), regulatory agencies, Institutional Review Boards (IRBs), and Pfizer processes.
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Provide Medical support and guidance for HIT initiatives including initial assessment, triaging opportunities for review, assessing organizational capabilities and feasibility, and providing clinical relevance to proposed HIT methodologies.
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