Scientist, Biostatistics

About the positionResponsibilities• Provide statistical input into the clinical development of drugs for treatment of cancer. • Work with the clinical team or assist other statisticians in designing clinical studies, authoring the statistical analysis plan, conducting the statistical analysis, and providing statistical input to the clinical study report. • Perform statistical analyses to support scientific presentations and manuscripts for individual studies/projects. • Participate in process improvement, training, standards development and enhancing statistical technical expertise.• Liaise with other statisticians within the organization, building working relationships with therapeutic area leaders, internal SAS programmers, clinical trial managers, and personnel from regulatory affairs, medical writing, and other disciplines as needed. Requirements• A Master's degree or higher in Statistics or related field is required. • Working knowledge of statistical software such as SAS and R is required. • Excellent verbal and written communication skills, including formal presentation skills are required.• Excellent analytical skills are required. Nice-to-haves• Experience and knowledge of Good Clinical Practices and regulatory requirements for clinical drug development, including the conduct of clinical trials is preferred. • Experience presenting to technical and lay groups at public meetings is preferred. • Experience working in the area of Oncology is a plus. Benefits• Medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.• 401(k) retirement plan. • Vacation - up to 120 hours per calendar year. • Sick time - up to 40 hours per calendar year. • Holiday pay, including Floating Holidays - up to 13 days per calendar year. • Work, Personal and Family Time - up to 40 hours per calendar year. Apply tot his job