Hopewell, New Jersey
Provide extensive biostatistical support in the planning, analysis and preparation of reports for clinical studies and for registering drugs in the U.S. and internationally. Work with senior staff members and clinical monitors in the design and conduct of clinical studies and evaluation. Interpretation and preparation of study results such that results can be presented in internal reports as well as in submission to the FDA and other regulatory agencies. Develop statistical programs as necessary to perform analysis, prepare data displays, verify data accuracy and validity.
Ph.D. in Biostatistics or Statistics with 0 to 3 years of experience, or a Masters Degree with 2 to 4 years of experience in the pharmaceutical industry. Must have demonstrated sound knowledge of major statistical software packages, SAS and Splus, and the ability to integrate statistical and biomedical concepts. Experience must include consulting with research personnel, including clinical researchers and authorship on formal reports and regulatory submissions, excellent communication and presentation skills, both written and verbal, are essential. Familiarity with ICH guidelines and FDA requirements is also required.
Position Type: Full Time
Reference Code: 01-UNFL-KS01
Please send resume, indicating reference code, to:
Bristol-Myers Squibb, Pharmaceutical Research Institute
P.O. Box 4000, Princeton, NJ 08543-4000
Fax: (609) 252-3242
Bristol-Myers Squibb Company is an equal opportunity employer. M/F/V/D