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Principal Biostatistician jobs at Incyte in United States, Wilmington
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Company (1)
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United States
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Wilmington
6 jobs found
19.09.2025
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Incyte Principal Biostatistician United States, Delaware, Wilmington
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Description:
Participate in the development and enforcement of SOPs and guidelines. Participate in pre-IND and NDA activities. Participate and contribute to authoring of Clinical Development Plan. Assist in writing relevant sections...
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04.09.2025
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Incyte Biostatistical Programmer Principal United States, Delaware, Wilmington
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Conduct statistical programming work of clinical data using SAS Software. Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with company SOPs....
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Full job details24.08.2025
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Incyte Principal Investigator DMPK United States, Delaware, Wilmington
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Serve as a DMPK project lead on discovery project teams. Initiate and engage in multifunctional collaborations to facilitate the advancement of drug candidates and build thorough knowledge of drug candidate...
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Full job details26.07.2025
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Incyte Principal Investigator Drug Product Technologies United States, Delaware, Wilmington
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Serve as a Medical Affairs lead and subject matter expert in dermatology. Develop, track, and report on goals, objectives, and outcomes aligned with organizational strategy. Deliver clear and balanced scientific...
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Full job details08.05.2025
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Incyte Principal/Sr Principal SAS programmer United States, Delaware, Wilmington
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Work independently to ensure the accuracy and quality of delivered results to satisfy the requirement of healthy authorities. Develop standard SAS macros for efficient analyses of clinical data which will...
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Full job details23.04.2025
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Incyte Principal/Sr Principal Investigator AI Driven Early Discover... United States, Delaware, Wilmington
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Designs novel core structures/key structural elements for a new project based on HTS leads or published literature compounds. Coordinates efforts with CROs for the acquisition and/or synthesis of compounds to...
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Full job detailsShare
Description:
Participate in the development and enforcement of SOPs and guidelines. Participate in pre-IND and NDA activities. Participate and contribute to authoring of Clinical Development Plan. Assist in writing relevant sections...
Expand description
Full job detailsThese jobs might be a good fit
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