Assoc. Dir. of Statistical Programming

The Associate Director will lead and manage Statistical Programming technical and functional responsibilities for selected clinical development programs and for company wide innovation and infrastructure building activities, including and quality and compliance initiatives. They will direct and implement analysis and reporting solutions for pre-clinical and clinical areas and for regulatory electronic clinical data submissions.


Manage activities of the group across project boundaries when appropriate.

Provide functional leadership and technical support to the group and project teams.

Help craft department goals and ensure linkage to personal goals in support of the corporate and departmental goals.

Monitors the activities of staff and provides them reliable guidance to succeed and grow.

Proactively makes recommendations to appropriate business units regarding the development and use of new tools and goals that further support and strengthen development capabilities.

Communicates company objectives to the group in a clear and timely manner.

Tunes group activities to company priorities, and adapts resources as needed, to ensure key goals are met on time.

Develops draft budgets and manages approved budgets for group(s).

Makes hiring decisions.

Seeks out and plans technical direction for the group and promotes technical innovation.

Performs other duties as assigned. Is required to supervise other Statistical Programming staff, with all incumbent supervisory responsibilities.






B.S. in Biostatistics, Statistics, Computer Science, or a related field and 10 plus years of SAS programming and relevant pharmaceutical industry experience. OR M.S. in Biostatistics, Statistics, Computer Science, or a related field and 8 plus years of SAS programming and relevant pharmaceutical industry experience.