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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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interpretation and be able to draw conclusions regarding progress and results of work, utilizing the data in appropriate decision making. Analytical problem solving. Gatthers input from colleagues, literature, and
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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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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
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-teams, and leaders. • Coordinate with other clinical research activities in the I&I RU and greater PRD organization. • Maintain up-to-date knowledge of scientific and clinical published literature in
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. Reviews literature as needed to respond to safety questions or those posed by the Safety Review Team, Data Monitoring Committee (DMC) or other individuals or bodies involved with the study. Communicates