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MIDD approaches can advance the understanding of pharmacological activity, efficacy and safety Provide support in the development and application of state-of-the-art quantitative methodologies
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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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for regulatory submissions. Knowledge of experimental design. Strong understanding of the state-of-the-art technologies to evaluate and leverage them for improved business processes. Aptitude to identify
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Review Team to evaluate medical benefits/risks to support targeted clinical indications. Reviews literature as needed to respond to safety questions or those posed by the Safety Review Team, Data
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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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. Provides technical trouble shooting support and interpretation of generated data. Reads scientific and technical literature to bring new and improved technologies and procedures to the laboratory
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to evaluate medical benefits/risks to support targeted clinical indications. Reviews literature as needed to respond to safety questions or those posed by the Safety Review Team, Data Monitoring Committee (DMC
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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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literature. May collaborate and author external publications and present research at external conferences. Qualifications Must-Have BS in Chemistry/Chemical Engineering with 9+ years of experience; MS in
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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