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team of an oncology program. ROLE RESPONSIBILITIES Acts as Clinical Pharmacology representative on Clinical Sub Team and Development Team, as appropriate. Provides the clinical pharmacology components
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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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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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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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. 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
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ROLE SUMMARY As a member of our Oncology team, you will play a critical role in supporting Translational Science Operations strategies, through scientific technical oversight and management
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labeling experience preferred). Bachelor's degree (in science or life sciences preferred) Attributes: Knowledge of global/regional regulatory guidelines and requirements important. Excellent written and
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at country or regional level Responsible for PTA and SIV report review for reports completed by the Site Care Partner Supports implementation of Pfizer's Site Technology Experience systems (e.g. Shared