Associate Clinical Science Director (Oncology)

The Associate Clinical Science Director designs, plans and develops clinical evaluation research studies in oncology with focus on solid tumors. This position assists in or prepares and authors clinical development related documents, summarizes study results, and supports project teams with scientific information.

Requirements

• Pharm.D., PhD, or M.D. or equivalent education and a minimum of five years of related experience.
• Equivalent combination of education and experience.
• Three to Five years of clinical development experience in the biotechnology or pharmaceutical industry or a combination of academia and industry.
• Participated in clinical oncology studies with molecular targeted or immunological therapies.
• Detailed knowledge of clinical trial implementation and drug development process.
• General knowledge of other related disciplines in the execution of clinical trials.
• Identifies and implements methods and procedures to achieve results with high quality.
• Performs a variety of complicated tasks with a wide degree of creativity and latitude.
• Has understanding and wide application of technical principles, theories, concepts, and techniques.
• Applies strong analytical and business communication skills.
• Highly organized and able to work under tight timelines
• Good public speaking and presentation 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