General Description:

Supporting early phase clinical development with a focus on solid tumors, the position will work with the clinical and regulatory team in designing clinical trials and developing the statistical analysis plan, facilitate the implementation of statistical analyses, provide statistical input to the study conduct, the CSR and scientific presentations/manuscripts, perform statistical analysis for submission related activities. The position will participate in process improvement, training, SOP development, and mentoring junior statisticians as a senior member of biostatistics department.

This individual will interface with clinical therapeutic area members, SAS programming, clinical data management, clinical operation, clinical pharmacology, medical writing and other functions.

Essential Functions of the job:

• A minimum of a Master Degree with 10+ years of experience or a PhD in Statistics or related field with 8+ years of experience in clinical drug development is required.

• Knowledge of SAS and/or R is strongly desirable.

• Experience with clinical trials and knowledge of regulatory guidance are required.

• Oncology experience is preferred but not required.

• Demonstrated written and oral communication skills.

• Ability to work within a team and work independently.

• Other important requirements include interdependent/analytic thinking skills, building strategic working relationships, and good decision-making capability.

Supervisory Responsibilities: NA

Education Required: Master’s Degree with at least 10 years’ experience, or Ph.D with at least 8 year experience

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.