at Incyte Corporation in Wilmington, Delaware, United States Job Description Provide statistical support to drug development programs. Participate in the development and enforcement of SOPs and guidelines. Participate in regulatory activities such as health authority meetings and submission related activities. Participate and contribute to authoring of Clinical Development Plan. Assist in writing relevant sections of the clinical study report. Interpret study results and provide review of statistical summary reports of study results for accuracy. Provide guidance and supervision to team members in authoring of analysis dataset specifications and programming of tables, listings, and figures. Monitor internal and CRO project activities including timelines, deliverables and availability of resources. Write and review statistical analysis plans. Provide statistical input to study protocols. Interact with members of the multidisciplinary project teams to establish project timelines. Manage and develop a diverse team of statisticians. Provide strategic input to drug development and the development of the biometrics department. Serve as a member of the biometrics management team, to manage and support drug development in Incyte.

Various worksites:

Hybrid, telecommuting permitted within area of intended employment, 3 days in office required. Ph.D. or foreign degree equivalent in Statistics, Mathematical Sciences, or related plus five years of related experience. Email resume to aguntz@incyte.com . Must reference job title and job code AD-XJ in the subject line. To view full details and how to apply, please login or create a Job Seeker account