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reviews, scientific exhibits and projects requiring skill in medical communication. Your planning skills will help in preparing forecasts for resource requirements, and providing areas of improvement
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utilized with full confidence in a compliant manner, these include: insights generation, field compensation, program performance calculation, SPP program performance, limited distribution network evaluation
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-making. Qualifications Minimum of bachelor's degree with 7+ years of experience, preferably in engineering, economics, statistics, computer science, or related quantitative field. Advanced degree with 3
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multidisciplinary project team of an oncology program. KEY RESPONSIBILITIES Act as Clinical Pharmacology representative on Clinical Sub Team and Development Team as appropriate. Participate in implementing model
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Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and controls (CMC) regulatory strategies for small and/or large molecules to meet global regulatory requirements
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advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply
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ROLE SUMMARY The Senior Manager, Auditor is responsible for the delivery and execution of the global Quality Assurance (QA) program audit activities on assigned GCP portfolio/programs/entities
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. Partner with other data science / computational groups to identify optimal solutions to scientific problems. Develop and deliver statistical training to scientists. Promote an effective Statistical network
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degree, preferably in a life science discipline. BS/BA +5 years, MS/MA +3 years, PhD +0 year s of experience in medical writing or related field. Understanding of the role of each member of cross
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ROLE SUMMARY The Senior Manager, Clinical Scientist (CS) will provide medical and scientific study and project support for multiple, global, Phase 1-4 vaccine clinical studies in a clinical program