Location: Berkeley Heights, NJ
Responsibilities will include, but are not limited to, the following:
Per Manager, 5 years of study statistician and managing and reporting of oncology study are preferred.
1. Contribute to efficient study design, preparing statistical consideration sections and providing input into other protocol sections.
2. Prepare statistical analysis plans including table shells.
3. Analyze clinical trial data; work with programmers to provide tables, listings and graphs, including ad hoc validation.
4. Review, synthesize, interpret and report analysis results.
5. Provide ad hoc data driven analyses. 6. Provide statistical input for the preparation of final study reports and other required documents.