Clinical Science Director
October 14
Description
•Designs, plans, and develops studies in early and/or late phase clinical oncology •Prepares and authors clinical development documents including study synopses and protocols •Summarizes study results for preparation of documents and publications •Supports project teams with scientific information and updates related to assigned clinical studies •Interacts with investigators and thought leaders in oncology •Collaborates with clinical operations and internal study team members •Participates in internal safety meetings and reports potential safety events •Contributes to the writing and/or review of product specific abstracts and presentations
Requirements
•Pharm.D., PhD, or M.D. •Minimum of 8 years of related experience or equivalent combination •5-8 years of clinical development experience in biotech or pharmaceutical industry •Experience in clinical oncology studies with molecular targeted or immunological therapies •Comprehensive knowledge of clinical trial implementation and drug development process •Strong analytical and business communication skills •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 for field sales staff •Opportunity to purchase company stock •Receive long-term incentives •15 accrued vacation days in the first year •17 paid holidays including a company-wide winter shutdown •Up to 10 sick days throughout the calendar year
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