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medical context required for benefit-risk assessments. Participates in the Safety Review Team to evaluate medical benefits/risks to support targeted clinical indications. Reviews literature as needed
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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 state-of-the-art hardware, software, and infrastructure support in a fast-paced and creative environment. How You Will Achieve It Design, execute, analyze and interpret high-throughput reaction screening
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development as a Clinical Research Investigator. Develops familiarity with the practice of pharmaceutical medicine through the literature and by attending appropriate trainings, meetings and conferences
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execution of regional studies for a development drug candidate Will contribute on transitioning projects or projects already transitioned Grows/maintains state of the art knowledge in the TA Representative
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execution of regional studies for a development drug candidate Will contribute on transitioning projects or projects already transitioned Grows/maintains state of the art knowledge in the TA Representative
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leader to join our team to build data foundations and tools to craft the future. You will design and implement scalable, extensible and highly-available data pipelines on large volume data sets, that will
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internal HTS capability within the Discovery Sciences department and its implementation. You will oversee the deployment of capital to assemble a state of the art screening infrastructure and build a
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leader to join our team to build data foundations and tools to craft the future. You will design and implement scalable, extensible and highly-available data pipelines on large volume data sets, that will