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biology or related field with established advanced capability and track record in developing and applying computational and bioinformatics methods. Five years or more of post-PhD academic and/or industry
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technical staff members on your own team and collaboratively. Qualifications Must-Have PhD with 2+ years of relevant experience Expertise in qPCR, digital PCR, DNA and RNA extraction, and experimental design
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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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analysis for multiple analyses supporting a program. Prepare formal presentations and written reports to Pfizer standards. Contribute to regulatory documents (summary documents, briefing books, regulatory
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Remain current in the scientific literature and state of the art techniques. Qualifications Must-Have Candidate should have a PhD in virology and/or immunology with at least 6+ years of relevant experience
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literature and regular maintenance of electronic notebooks. Qualifications Must-Have PhD in Biology, Neuroinflammation, Neuroscience or other related discipline or MS with 7+ years of relevant molecular and
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research/discovery work is conducted with highest quality and ethical guidelines and in accordance with relevant regulatory, QC, and compliance guidelines. Qualifications: PhD with a minimum of 2 years
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) and 13+ years of experience in the biopharmaceutical industry OR PhD/PharmD and 10+ years of regulatory submission experience in the biopharma industry. 5+ years of people management experience
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) Development and Oversight at disease area and program level including integration within the Quality Management System (QMS ), and ensuring individual asset and study level IQMPs are in place. Escalation
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development strategy and program execution of research projects with a particular focus on obesity and associated conditions (e.g., cardiovascular disease, renal impairment, diabetes, etc.), and lead