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translation of pre-clinical observations into clinical experiments and studies designed to demonstrate proof of pharmacology, proof of mechanism and proof of concept for new candidate medicines. The CL will
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. QUALIFICATIONS Basic Qualifications PhD in Molecular or Cellular Biology, Biochemistry, Genetics/Genomics, Pharmacology, or related field with typically 3+ years of relevant postdoctoral experience in an academic
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biology expertise; take a proactive role in personal growth and scientific development. QUALIFICATIONS Basic Qualifications PhD or MD/PhD in Molecular or Cellular Biology, Genetics, Pharmacology (or a
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Immunology Research Unit (I&I RU) (Discovery, Pre-clinical and Systems Immunology), Clinical Pharmacology and Bioanalytics, Statistics, and Research and Developments (PRD) teams by maintaining open
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outside Research, such as Clinical Pharmacology and Precision Medicine, Pharmaceutical Sciences, Early and Late Clinical Development, Legal/IP, Regulatory Strategy, and Project & Portfolio Management
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groups within and outside Research, such as Clinical Pharmacology and Precision Medicine, Pharmaceutical Sciences, Early and Late Clinical Development, Legal/IP, Regulatory Strategy, and Project
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Non-clinical Project Leaders, the RPM continues driving implementation of non-clinical pharmacology activities through registration. The RPMs will be responsible for keeping project information (e.g