Associate Biostatistics Director (Biotech, Oncology)

Applies extensive technical expertise and experience to provide written and verbal recommendations on statistical issues, design and conduct of clinical trials of all phases. Works collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials.

Requirements

• MS/MA degree in related discipline and a minimum of 9 years of related experience
• PhD in related discipline and a minimum of 5 years of related experience
• Equivalent combination of education and experience
• Experience in oncology and study Phases I-III highly preferred
• Experience in Biotech/Pharmaceutical industry preferred
• Experience with managing CROs in the conduct of clinical trials
• Strong SAS programming knowledge
• Guides the successful completion of major programs, projects and/or functions
• Develops technical and/or business solutions to complex problems
• Identifies and implements methods, techniques, procedures, and evaluation criteria to achieve results
• Performs a variety of complicated tasks with a wide degree of creativity and latitude
• Has complete understanding and wide application of technical principles, theories, concepts, and techniques
• Has good general knowledge of other related disciplines
• Applies strong analytical and business communication skills

Benefits

• 401k plan with generous company contributions
• Group medical, dental and vision coverage
• Life and disability insurance
• Flexible spending accounts
• Discretionary annual bonus program
• Sales-based incentive plan
• Opportunity to purchase company stock
• Long-term incentives
• 15 accrued vacation days in the first year
• 17 paid holidays including a company-wide winter shutdown in December
• Up to 10 sick days throughout the calendar year