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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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management as it relates to driving labeling process in regulated industry MS Office Suite; expert formatting skills (Word, XML) Bachelor's degree (in science or life sciences preferred) Attributes: Knowledge
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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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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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-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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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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-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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. 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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documents Facilitate team and cross functional meetings. Education Qualifications: Bachelor's degree in a science or life sciences required 3+ years experience in a regulated environment; pharmaceutical