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Jobs at Incyte in United Kingdom
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16 jobs found
23.08.2025
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Incyte Senior Medical Writer United Kingdom, England, South Somerset
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Develop regulatory documents for submission to regulatory agencies globally, in accordance with ICH and other global guidelines, standards and processes, and Company authoring standards, as applicable, in adherence with study/project...
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23.08.2025
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Incyte Senior/ Executive Medical Director United Kingdom, England, South Somerset
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Leads development efforts for assets post-candidate selection through first in human trials, including early dose escalation, safety and tolerability evaluation, dose selection, translational medicine (proof of mechanism studies) and proof...
26.07.2025
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Incyte Senior Clinical Operations Lead United Kingdom, England, South Somerset
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Assists in the review, development and writing of clinical trial documents and manuals, including but not limited to study manuals, laboratory or biomarker plans, and other supporting documents. Create Master...
25.07.2025
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Incyte Senior Clinical Operations Lead United Kingdom, England, South Somerset
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Assists in the review, development and writing of clinical trial documents and manuals, including but not limited to study manuals, laboratory or biomarker plans, and other supporting documents. Create Master...
12.07.2025
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Incyte Immunology Business Director- Northwest United Kingdom, England, South Somerset
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Lead cross-functional teams in the development, revision, review, and approval of CCDS and local labeling documents in compliance with regulatory and internal standards. Author new and/or revised CCDS, USPI and...
28.06.2025
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Incyte Medical Director United Kingdom & United Kingdom, England
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The main purpose of the job is to lead the UK and Ireland Medical Affairs group on the hematology portfolio, strategically and operationally. The role provides medical insights on currently...
25.05.2025
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Incyte Senior Director/ Director Clinical Research Scientist United Kingdom, England, South Somerset
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Development of protocols for clinical studies. Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans. Drafting and review of clinical...
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Description:Full job details
Develop regulatory documents for submission to regulatory agencies globally, in accordance with ICH and other global guidelines, standards and processes, and Company authoring standards, as applicable, in adherence with study/project...
These jobs might be a good fit
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