at Incyte Corporation in Wilmington, Delaware, United States
Job Description
Responsible for providing statistical support for drug development programs in all phases of development. Establish project timelines with members of the multidisciplinary project teams. Provide statistical input to study protocols and write statistical analysis plans. Monitor internal and CRO project activities including timelines, deliverables, and availability of resources. Provide guidance and supervision to programmers in authoring analysis dataset specifications and programming of tables, listings, and figures. Interpret study results and provide review of statistical summary reports of study results for accuracy. Write relevant sections of the clinical study report. Contribute to authoring of the clinical development plan. Participate in pre-IND and NDA activities. Participate in the development and enforcement of SOPs and guidelines.
Requires PhD degree or foreign equivalent in Statistics, Biostatistics, or related field.
E-mail resume to Anne Guntz (aguntz@incyte.com). Must reference job title and job code PB-SL in the subject line.
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Job Posting:
1235426
Posted On:
Feb 01, 2024
Updated On:
Mar 05, 2024
