Position title will be based on experience level of candidate and range from junior to senior levels. Responsible for statistical aspects of pre-clinical through Phase IV clinical trials, including experimental design, protocol development, statistical analyses, writing statistical contributions to clinical reports and collaborating with clinical investigators, physicians and medical writers. Serve as a consulting statistician for various teams, play a key role in preparing research reports and NDA submissions for various drugs. Many therapeutic areas, including CNS, GI, Oncology, Cardio, Respiratory and HIV/AIDS.Very good oral and written communication and negotiation skills.
Minimum Requirements: MS plus 2 - 9 years experience or a PhD with 0 - 5 years experience. Degree must be in statistics or in mathematics with a large statistical component.
- Level and title will be commensurate with the education and experience level of the selected candidate.
