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engineering controls and target product attributes are met . Support data review and present learnings post- manufactu re . D rive the timely resolution of quality deviations and assist in root cause analysis
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with brand strategies to support successful pre-launch, launch, post-launch medical initiatives. ROLE RESPONSIBILITIES Product Strategy and Brand Plan Development: Oversee and coordinate medical input
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symposia & congress planning Ability to contribute to Publication Planning, data generation activities and other medical/scientific activities related to informing HCPs on proper use of this potential new
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. Support a high functioning and performance culture for team QUALIFICATIONS MD or DO (Lung Cancer background preferred) Experienced in the diagnosis and treatment of patients with lung cancer within the US
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health economics in HEOR projects involving clinical trials and observational studies, including those in development supporting drug approval and reimbursement, HTA, as well as other post-approval
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, e.g., GDMS. Finalize documents post QC (including update of GDMS document properties such as entry of PfLEET2 number, update of document title, update CDS cover page etc.). Manage the document status in
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clinical development and commercial priorities for Pfizer Oncology. QUALIFICATIONS: Education MD, MD/PhD or equivalent with extensive clinical experience. Experience 10+ years of oncology development
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with brand strategies to support successful pre-launch, launch, post-launch medical initiatives. ROLE RESPONSIBILITIES Product Strategy and Brand Plan Development: Oversee and coordinate medical input
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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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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