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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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-if scenario analyses in Planisware (base, optimistic and pessimistic development) based on context derived from the Program Manager / Director and project team members (e.g. Pharmaceutical Sciences, Clinical
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groups (Disease Biology, Chemistry, Computational Biology, Structural Biology, Primary Pharmacology), be adept at building partnerships, and be very team-oriented. Highly motivated, highly organized and
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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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Bachelor of Science degree in Engineering, Biology, Chemistry, Pharmacology, Computer Science or a related field with 6+ years of relevant experience. Excellent organization and planning skills and the
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Job Summary: The Senior Scientist Computational Biologist will be a key member of the Machine Learning and Computational Sciences Team, focusing on the analysis and interpretation of complex
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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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JOB SUMMARY . • Clinical Development expert focused on the execution of clinical studies and brings that expertise to the design & conduct of clinical studies in alignment with the program and