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other therapeutic areas such as immunology and inflammation, metabolic diseases, and infectious diseases. Responsibilities: Work closely with multidisciplinary project teams to develop and implement
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able to operate independently on project teams, although, may need instruction on more complex or unusual study challenges and/or tasks. Serve as technical support for clinical issues raised by internal
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making and implementation. Provide education on the clinical and economic impact to help inform customer decision-making and improve population health through the communication of real-world data analyses
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ROLE SUMMARY Develop data infrastructure for data scientists and ensure appropriate and efficient development of care gap and HCP prioritization models ROLE RESPONSIBILITIES Develop and maintain
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expertise required for project progression. The individual will also work closely with the Medicinal Chemistry and Oncology Biology groups to innovate and develop the next-generation of therapies. ROLE
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regulatory interactions and filings Develop manuscripts, abstracts and presentations for scientific meetings Evaluate safety, pharmacology, and efficacy data from ongoing and completed studies to inform
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study subjects as needed. Process samples for analysis and storage and oversee the specimen storage inventory. Perform safety inspection of laboratories and surrounding office area as assigned and prepare
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- and late-phase clinical trials. The Scientist will be responsible for working with fellow scientists to develop robust, efficient, scalable strategies for improving process performance. With your deep
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maintenance. In addition, the associate scientist may train other analysts. All work is to be performed in a compliant manner, according to applicable standard operating procedures (SOP) and cGxP guidelines, as
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, digital platforms, and content for newly prioritized medical channels Chair Scientific Publication Committees and Medical Content Dissemination Subteams for assigned compound(s) to develop global