Director Sr Business Development 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
16 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...
Maintaining primary and secondary cell lines for further work in assays and biology experiments. Able to conduct assays semi independently and make sound judgements about selecting technical approaches but requires...
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...
Development of protocols for clinical studies. Preparation of clinical development plans. Drafting of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Annual Reports and other FDA submissions. Monitor,...
Crystallography experience is required. Cryo-EM experience is desirable, but not required. Requires good skills on recombinant protein purification, crystallization and structure determination. Help troubleshooting recombinant protein expression and purification. Protein...
Design, develop and execute biochemical and biophysical assays of various formats to support high throughput confirmation, qualification, and optimization of AI generated hits, including compounds of different affinities and/or of...
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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