Senior Manager/associate Director Contract Operations jobs at Incyte in United States, Wilmington
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Company (1)
Job type
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Job title (1)
United States
State
Wilmington
18 jobs found
25.05.2025
I
Incyte Associate Director Global Regulatory Affairs United States, Delaware, Wilmington
Manage the creation, review, and submission of regulatory documents (new protocols, new investigators, adverse events, periodic and annual reports, Development Safety Update Reports, nonclinical and clinical study reports, summary documents...
Governance and Maintenance of all Templates and Clause Library configured into CLM. Govern and maintain contract templates. Collaborate with Legal Counsel and other relevant functional area stakeholders, as it relates...
Deliver therapeutic information on products in line with marketing strategy. Promote INCYTE IAI Dermatology product to prescribing Dermatologist specialists in compliance within compliance and legal requirements and according to the...
Deliver therapeutic information on products in line with marketing strategy. Promote INCYTE IAI Dermatology product to prescribing Dermatologist specialists in compliance within compliance and legal requirements and according to the...
Conduct process analysis, simplification and intensification for APIs and their intermediates. Plan how to move laboratory synthetic procedures into a pilot production phase, then onto large-scale industrial processing. Develop methods...
Support activities required within process chemistry, pharmaceutical and analytical development to ensure submission readiness of drugs into international markets. Manage the GMP/GDP readiness of new products for international markets. Provide...
Conduct search and evaluation activities to identify pharmaceutical licensing opportunities and strategic collaborations in key therapeutic areas of strategic interest, including immunology and auto-immunity, oncology and dermatology. Lead the assessments...
Manage the creation, review, and submission of regulatory documents (new protocols, new investigators, adverse events, periodic and annual reports, Development Safety Update Reports, nonclinical and clinical study reports, summary documents...
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