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with project teams to establish screening strategies, interpret results, and make decisions to drive programs forward. Write protocols, maintain ELN, and regularly review literature to m aintain
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clinical strategy Conduct literature reviews and prepare summaries to support clinical development strategies Support ongoing study activities and collaborate across functions for study level deliverables
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for scientific meetings and advisory boards. Conduct literature reviews and prepare summaries to support clinical development programs. Medical resource for design and interpretation of clinical and preclinical
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to review literature to formulate new ideas and have the ability to work independently as well as with an interdisciplinary team of scientists in a highly collaborative environment. The candidate will have
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Ability to work in a virtual work environment Skilled at utilizing medical literature and drug information databases Proficient at critically evaluating literature and writing/summarizing clinical and
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skills. Creative, self-motivated and the ability to work independently including analysis and troubleshooting of experimental results and reviewing literature to formulate new approaches. Nice-to-Have
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for scientific meetings and advisory boards. Conduct literature reviews and prepare summaries to support clinical development programs. Medical resource for design and interpretation of clinical and preclinical
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statisticians. An ideal candidate should be: 1. proficient in the use state-of-the-art tools for genomic data analysis, integration and visualization, 2. have a solid understanding of the principles and